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 3004610460.
Baxter Pharmaceuticals India Pvt Ltd
Ahmedabad, -, India
Issue DateAugust 04, 2017
FEI Number3004610460
CountryIndia
Status
1 Related Warning Letter
Product Type
Drugs
Establishment Type
Finished Pharmaceutical Manufacturer
Baxter Pharmaceuticals India Pvt Ltd FDA Form 483, Ahmedabad, August 4, 2017
