Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3009724085.
Olympia Pharmaceuticals
Orlando, Florida, United States
Issue DateMarch 02, 2022
FEI Number3009724085
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Producer of Sterile Drug Products
Olympia Pharmaceuticals FDA Form 483, Orlando, Florida, March 2, 2022
