FDA Inspection 937613 — 5N Plus Lubeck GmbH

5N Plus Lubeck GmbH — FEI 3002807159

The FDA completed an inspection of 5N Plus Lubeck GmbH on August 7, 2015 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
August 7, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lubeck (Germany)