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GERI-GENTLE CORPORATION Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3012227494.

GERI-GENTLE CORPORATION

South Plainfield, New Jersey, United States
Issue DateDecember 04, 2017
FEI Number3012227494
CountryUnited States
Status
No Warning Letter
Product Type
Devices
GERI-GENTLE CORPORATION FDA Form 483, South Plainfield, New Jersey, December 4, 2017