Home / Inspections / 857318

FDA Inspection 857318 — Haupt Pharma Amareg GmbH

Haupt Pharma Amareg GmbH — FEI 3008293991

The FDA completed an inspection of Haupt Pharma Amareg GmbH on November 22, 2013 in Ratisbon. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 22, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ratisbon (Germany)

Facility

Other inspections at this facility

  • 1274881 (VAI Fri Jul 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1134674 (VAI Fri Jun 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1038904 (VAI Fri Nov 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 986248 (VAI Fri Aug 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 727709 (NAI Wed May 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources