FDA Inspection 612343 - Gendron Inc. - September 11, 2009

Record Details

This FDA Inspection record concerns Gendron Inc., with an inspection on September 11, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Gendron Inc.
Inspection Date: September 11, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d9ce86b3-43cf-4c85-adb3-b7c05b4bd2a1

Violation Codes3

21 CFR 820.100(a)21 CFR 820.2221 CFR 820.40(a)

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