FDA Inspection 600292 - Merete GmbH - July 02, 2009

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Record Details

This FDA Inspection record concerns Merete GmbH, with an inspection on July 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Merete GmbH
Inspection Date: July 2, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 58ac488c-35b4-4dfd-8dc6-8a5453f5b401

Violation Codes4

21 CFR 803.1721 CFR 820.30(e)21 CFR 820.70(c)21 CFR 820.80(c)

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