FDA Inspection 1012240 — Excella GmbH & Co. KG

Excella GmbH & Co. KG — FEI 3000242652

The FDA completed an inspection of Excella GmbH & Co. KG on March 17, 2017 in Feucht. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Feucht (Germany)