FDA Inspection 831545 — Eurofins PHAST GmbH

Eurofins PHAST GmbH — FEI 3005909718

The FDA completed an inspection of Eurofins PHAST GmbH on Apr 30, 2013 in Homburg. 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
Apr 30, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Homburg (Germany)