FDA Inspection 1074936 — 5N Plus Lubeck GmbH

5N Plus Lubeck GmbH — FEI 3002807159

The FDA completed an inspection of 5N Plus Lubeck GmbH on November 9, 2018 in Lubeck. 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, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lubeck (Germany)