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 3004021253.
Apitoria Pharma Private Limited
Doultabad, -, India
Issue DateAugust 12, 2021
FEI Number3004021253
CountryIndia
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Active Pharmaceutical Ingredient Manufacturer
Apitoria Pharma Private Limited FDA Form 483, Doultabad, August 12, 2021
