FDA Inspection 833173 — Jungbunzlauer Ladenburg Gmbh

Jungbunzlauer Ladenburg Gmbh — FEI 3002807365

The FDA completed an inspection of Jungbunzlauer Ladenburg Gmbh on May 10, 2013 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
May 10, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ladenburg (Germany)