FDA Inspection 1033906 - GERI-GENTLE CORPORATION - December 04, 2017

Record Details

This FDA Inspection record concerns GERI-GENTLE CORPORATION, with an inspection on December 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: GERI-GENTLE CORPORATION
Inspection Date: December 4, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9151ad5b-ecf3-45ba-b588-75aa4ac504e1

Violation Codes6

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.15021 CFR 820.198(a)21 CFR 820.50(a)21 CFR 820.80(b)

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