SAMPLE COMPANY                                        Page 1 of 2
SOP # 10-2  Revision: 0                Prepared by:             _
Effective Date:                        Approved by:             _


Title:         IN-PROCESS AND FINAL INSPECTION AND TESTING

Policy:   As part of the company's total quality assurance
          program, quality control checks will be performed at
          various completion levels during production and upon
          final completion of the product in accordance with
          specified requirements and/or as outlined in the
          quality plans.

Purpose:  To outline the activities and responsibilities for
          quality control inspections of products.

Scope:    This procedure applies to all products manufactured by
          the company.


Procedures:

1.0  Assembly

1.1  The QC Manager will periodically review production in
     process to ascertain that items are being produced in
     compliance with applicable design and manufacturing
     documents contained in the Master Product Record.  These
     documents can include; quality plans, inspection/test
     instructions, assembly manuals or instructions, bill of
     materials, drawings, specification sheets, sample model
     components/products, etc.

1.2  When appropriate as indicated by the quality plan, quality
     inspection and approval identification will be stamped onto
     the component/product or on supporting check-out
     documentation.


2.0  Finished Goods

2.1  All products manufactured by the company shall be tested and
     inspected for proper assembly and function.

2.2  QC Check Out Sheets determined in the design process (see
     SOP on Preproduction Quality and Planning) for each product
     will be utilized to determine appropriate items and
     inspection/testing parameters to be followed.

2.3  Upon satisfactory completion of the inspection process, the
     applicable QC Check Out Sheet will be signed, dated and
     filed as required.
IN-PROCESS AND FINAL INSPECTION AND TESTING           Page 2 of 2


3.0  Nonconformance and Disposition

3.1  If a finished product or sub-assembly is rejected for any
     reason during the QC process, the product or component will
     be red-tagged and segregated by placing in quarantine to
     await disposition according to the procedure for Control of
     Nonconforming Product.