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FDA Inspection 1156166 — G. Pohl-Boskamp GmbH & Co. KG

G. Pohl-Boskamp GmbH & Co. KG — FEI 3002807915

The FDA completed an inspection of G. Pohl-Boskamp GmbH & Co. KG on August 28, 2020 in Hohenlockstedt. 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
August 28, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hohenlockstedt (Germany)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1264909 (VAI Thu Sep 14 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025477 (VAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 957110 (VAI Thu Feb 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 935101 (NAI Fri Jul 03 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 826846 (VAI Fri Feb 22 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources