FDA Inspection 649113 — Jungbunzlauer Ladenburg Gmbh

Jungbunzlauer Ladenburg Gmbh — FEI 3002807365

The FDA completed an inspection of Jungbunzlauer Ladenburg Gmbh on Feb 11, 2010 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
Feb 11, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ladenburg (Germany)