FDA Inspection 1075113 — Jungbunzlauer Ladenburg Gmbh

Jungbunzlauer Ladenburg Gmbh — FEI 3002807365

The FDA completed an inspection of Jungbunzlauer Ladenburg Gmbh on Nov 22, 2018 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
Nov 22, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ladenburg (Germany)