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FDA Inspection 1000875 — Vetter Pharma Fertigung GmbH & Co. KG

Vetter Pharma Fertigung GmbH & Co. KG — FEI 3002270322

The FDA completed an inspection of Vetter Pharma Fertigung GmbH & Co. KG on January 17, 2017 in Ravensburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ravensburg (Germany)

Facility

Other inspections at this facility

  • 1241531 (VAI Wed Jul 13 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1129698 (NAI Wed Sep 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 931820 (VAI Tue Jan 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 895499 (NAI Tue Jul 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 863242 (VAI Thu Dec 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources