FDA Inspection 1290170 — Jungbunzlauer Ladenburg Gmbh

Jungbunzlauer Ladenburg Gmbh — FEI 3002807365

The FDA completed an inspection of Jungbunzlauer Ladenburg Gmbh on Aug 3, 2022 in Ladenburg. 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
Aug 3, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ladenburg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)