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 3004086884.
Apitoria Pharma Private Limited
Sangareddy District, -, India
Issue DateOctober 25, 2019
FEI Number3004086884
CountryIndia
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Active Pharmaceutical Ingredient Manufacturer
Apitoria Pharma Private Limited FDA Form 483, Sangareddy District, October 25, 2019
