FDA Inspection 782066 — Eurofins Lancaster Laboratories, LLC

Eurofins Lancaster Laboratories, LLC — FEI 2513291

The FDA completed an inspection of Eurofins Lancaster Laboratories, LLC on May 17, 2012 in Lancaster, PA. 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
May 17, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lancaster, PA (United States)