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 3006370489.
Apitoria Pharma Private Limited
Sangareddy, -, India
Issue DateNovember 18, 2022
FEI Number3006370489
CountryIndia
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Drug Substance Intermediate Manufacturer
Apitoria Pharma Private Limited FDA Form 483, Sangareddy, November 18, 2022
