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FDA Inspection 811631 — 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 November 9, 2012 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
November 9, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ravensburg (Germany)

Facility

Other inspections at this facility

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  • 1129698 (NAI Wed Sep 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1000875 (VAI Tue Jan 17 2017 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))

FDA data resources