FDA Inspection 970977 — Jungbunzlauer Ladenburg Gmbh

Jungbunzlauer Ladenburg Gmbh — FEI 3002807365

The FDA completed an inspection of Jungbunzlauer Ladenburg Gmbh on May 12, 2016 in Ladenburg. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 12, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ladenburg (Germany)