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LEESAR, INC 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 3010166880.

LEESAR, INC

Fort Myers, Florida, United States
Issue DateJuly 12, 2017
FEI Number3010166880
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
LEESAR, INC FDA Form 483, Fort Myers, Florida, July 12, 2017