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FDA Inspection 1109935 — Eurofins BioPharma Product Testing Hamburg GmbH

Eurofins BioPharma Product Testing Hamburg GmbH — FEI 3010166293

The FDA completed an inspection of Eurofins BioPharma Product Testing Hamburg GmbH on September 18, 2019 in Hamburg. 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
September 18, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hamburg (Germany)

Facility

Other inspections at this facility

  • 1288412 (VAI Wed Oct 19 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841999 (NAI Wed Jul 10 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources