FDA Inspection 1248219 — Lichtenheldt Gmbh Pharmazeutische Fabrik

Lichtenheldt Gmbh Pharmazeutische Fabrik — FEI 3002853327

The FDA completed an inspection of Lichtenheldt Gmbh Pharmazeutische Fabrik on Feb 17, 2022 in Wahlstedt. 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
Feb 17, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wahlstedt (Germany)

Additional Details

Mutual Recognition Agreement (MRA)