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 3007197995.
Shilpa Pharma Lifesciences Limited
Chicksugur, Raichur, -, India
Issue DateJuly 26, 2019
FEI Number3007197995
CountryIndia
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Active Pharmaceutical Ingredient Manufacturer
Shilpa Pharma Lifesciences Limited FDA Form 483, Chicksugur, Raichur, July 26, 2019
