Source: FDA, document on file. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3009883410.
Observations3
Issue DateMarch 06, 2018
Status2 Related Warning Letters
Establishment TypeHuman Drug Manufacturer
Related Inspections6
Establishment Details
Firm
EUGIA Pharma Specialities Limited
Issued To
Auronext Pharma
Location
Riico Industrial Area, -, India
FEI Number
3009883410
Establishment Type
Human Drug Manufacturer
Product Type
Drugs
Issue Date
March 06, 2018
Country
India
Inspection History, 2015 to 2025
VAI4
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
Talk to a Specialist