Product ID, Inspection and Test Status, - QS9000

B

Becky Blosser

#1
Must nonconforming/quarantined goods be visibly marked?

Our company has been marking quarantined goods with a special label. We have not been able to set aside marked areas for quarantined product, as space is at a premium and goods are stored in the first available space.

However, since the process started, we have upgraded our computer system and added RF scanners to scan location and counts directly into the system. A suggestion has been made that the quarantine ID be shown on the scanners, so that Team Members will know that the product is not available for shipment, and eliminate the time-consuming process of attachment of the labels.

Would this be kosher, or must there be a physical, visible ID?
 
Elsmar Forum Sponsor
B

Becky Blosser

#3
Well, duh! On my part, that is! :eek:

I was looking in the wrong place (as usual, it seems). I researched 4.12 - apparently I forgot to think about quarantined product as nonconforming.

Thanks for the guidance!
 
A

Al Dyer

#4
Becky:

Remember, quarantined product does not automatically mean nonconforming product.

We have special shipments of goods and products that we want to control in a different manner than nonconforming product.

ASD...
 
Thread starter Similar threads Forum Replies Date
K Final Inspection for Software Product - Functional Test? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
Douglas E. Purdy How AQL Inspection & Test corresponds to Control of Nonconforming Product AQL - Acceptable Quality Level 11
T Nonconforming product at customer detected by a routine inspection by field service Nonconformance and Corrective Action 9
V Handling decomissioned line/equipment during 1st time product-based inspection US Food and Drug Administration (FDA) 1
L Who and when to determine AQL for our product inspection AQL - Acceptable Quality Level 1
S Any advice for my Pre Approval Inspection (PAI) for Combination product ? US Food and Drug Administration (FDA) 1
H Writing a Product Label Inspection Work Instruction Manufacturing and Related Processes 2
T System Corrective Actions when Conforming Product depends heavily on Inspection Nonconformance and Corrective Action 3
W FDA Preapproval Inspection - Submitting a 505b2 for a combination product to the FDA Other US Medical Device Regulations 5
L How to standardize inspection plan for diversify product Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
W Authorizing Product Release while Eliminating In-Process Inspection Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
R Layout Inspection and Functional Testing - "Product" in 8.2.4.1 Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
V Who can perform inspection of product? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 25
T Final inspection and testing of product from validated processes Misc. Quality Assurance and Business Systems Related Topics 1
W How to make a Product Specification Summary / Quality Inspection Sheet Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
P First Article Inspection - FAI for every new product launch AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
D CSA Inspection - Process equipment shipped elsewhere to process product Various Other Specifications, Standards, and related Requirements 9
S Layout inspection - product family approach? IATF 16949 - Automotive Quality Systems Standard 2
Z Shall we only control the Inspection card of the most assembled Product? Document Control Systems, Procedures, Forms and Templates 1
R Product Status Identification after receiving inspection? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
S First Article Inspection in an AS9100 service industry (Final product non tangable) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 13
S NonConforming product NCR during Manufacturing vs. NCR only at final inspection AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 21
B Can I do layout inspection and product audit at the same time and plan? IATF 16949 - Automotive Quality Systems Standard 5
D Implementing Operator Product Self-Inspection Inspection, Prints (Drawings), Testing, Sampling and Related Topics 26
A Where's the value add in product audits when your process is inspection based? IATF 16949 - Automotive Quality Systems Standard 9
S Definition Product Audit (8.2.2.3) vs. Layout Inspection (8.2.4.1) - What are the differences? Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 8
S P-Chart Question - Need Guidance - 100% inspection of all product parts required? Statistical Analysis Tools, Techniques and SPC 11
K Probability of passing bad product - Air decay inspection Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
A Layout Inspection & Product inspection - Can We Eliminate Product Audit? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
B Product inspection specification sheet form - Examples needed Inspection, Prints (Drawings), Testing, Sampling and Related Topics 10
W Product Audits must include raw material or incoming inspection process? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 14
R 8.2.3.1 Monitoring and measurement - Containment of product and 100% inspection Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
N Incoming Product Quality - Receiving inspection for chemical substance Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
JoCam On-product labels for Medical Devices EU Medical Device Regulations 3
Awais How to mistake proof - Shipping Orders with Shortages - Product Quantity Accountability mismatch with Job Traveller? Manufacturing and Related Processes 17
L Product and process Deviation procedure Manufacturing and Related Processes 1
H Using/Selling power banks with your product as a "mobile version" CE Marking (Conformité Européene) / CB Scheme 3
H Electronic care product on patient bed side - Flammability requirements (62368-1) Hospitals, Clinics & other Health Care Providers 0
B Design Responsibilities for Mature Acquired Product Lines ISO 13485:2016 - Medical Device Quality Management Systems 3
D Dental application - medical product or not? Other US Medical Device Regulations 8
Q Product Quality vs Product Defects Manufacturing and Related Processes 4
J Verification of purchased product / supplier questionnaires ISO 13485:2016 - Medical Device Quality Management Systems 2
E Any template/ form of Monitoring and Measurement of Processes and product to ISO 13485? ISO 13485:2016 - Medical Device Quality Management Systems 1
S Product Code 510(k) exemption US Food and Drug Administration (FDA) 1
M REACH assessment of PCBA/finished product REACH and RoHS Conversations 2
J Validity of CE mark on distributed product when company ceases trading EU Medical Device Regulations 3
Q News cradle to grave - Product life cycle ISO 14001:2015 Specific Discussions 5
J Using of CE marking - Two CE markings on the product CE Marking (Conformité Européene) / CB Scheme 5
W Final Report re: Market withdrawal of radiation-emitting product Other US Medical Device Regulations 0
M Combination Product - New MAA EU Medical Device Regulations 0

Similar threads

Top Bottom