FDA Inspection 707238 — Eurofins Lancaster Laboratories, LLC
The FDA completed an inspection of Eurofins Lancaster Laboratories, LLC on Jan 25, 2011 in Lancaster, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 25, 2011
- Fiscal Year
- 2011
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Lancaster, PA (United States)