FDA Inspection 1074936 — 5N Plus Lubeck GmbH

5N Plus Lubeck GmbH — FEI 3002807159

The FDA completed an inspection of 5N Plus Lubeck GmbH on Nov 9, 2018 in Lubeck. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 9, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lubeck (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.