FDA Inspection
GERI-GENTLE CORPORATIONFDA 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.
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ID · 8209fa02-a4cb-4a05-bd1b-c63eaa45d449
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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