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 3004611182.
Apitoria Pharma Private Limited
Pydibhimavaram, -, India
Issue DateAugust 02, 2022
FEI Number3004611182
CountryIndia
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Active Pharmaceutical Ingredient Manufacturer
Apitoria Pharma Private Limited FDA Form 483, Pydibhimavaram, August 2, 2022
