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 3008461619.
Eugia Pharma Specialities Limited
Pashamylaram, -, India
Issue DateFebruary 20, 2018
FEI Number3008461619
CountryIndia
Status
2 Related Warning Letters
Product Type
Drugs
Establishment Type
Human Drug Manufacturer
Eugia Pharma Specialities Limited FDA Form 483, Pashamylaram, February 20, 2018
