Need some guidance on how to report non-compliance and the corrective action taken to the member states in the EU.
Hi Ronen,The MDD clauses that come to my mind only speak of your obligation to notify competent authorities when an adverse event has occurred or you have initiated a recall to prevent potetial adverse events. Is that the situation you were referring to?
Could you please state the MDD clause that raised your concern?
manufacturers who consider or have reason to believe that EEE which they have placed on the market is not in conformity with this Directive immediately take the necessary corrective measures to bring that EEE into conformity, to withdraw it or recall it, if appropriate, and immediately inform the competent national authorities of the Member States in which they made the EEE available to that effect, giving details, in particular, of the non- compliance and of any corrective measures taken;
Also found ROHS member state contact information, so I was puzzled ...who to contact...at the moment thinking abt sticking to the Contacts in European Commission. Any inputs?