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Tedor Pharma, 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 3003855180.

Tedor Pharma, Inc.

Cumberland, Rhode Island, United States
Issue DateApril 20, 2017
FEI Number3003855180
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Tedor Pharma, Inc. FDA Form 483, Cumberland, Rhode Island, April 20, 2017