FDA Inspection
Eurofins Lancaster Laboratories, IncEurofins Lancaster Laboratories, Inc – FDA Inspection, Oct 6, 2009
Record Details
This FDA Inspection record concerns Eurofins Lancaster Laboratories, Inc, with an inspection on October 6, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- October 6, 2009
- Product Type
- Drugs
View Company Profile
ID · 28f6d683-eeef-4e09-8a37-3028ff535f1f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 631027
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Eurofins Lancaster Laboratories, Inc
13| Date | Classification | Office | Project area |
|---|---|---|---|
| September 23, 2025 | Not classified | Philadelphia District Office | |
| August 26, 2025 | VAI | Philadelphia District Office | Drug Quality Assurance |
| October 21, 2021 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 17, 2019 | NAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| September 13, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Eurofins Lancaster Laboratories, Inc
- FDA Inspection 1284580 - 2025-09-23
- FDA Inspection 1279557 - 2025-08-26
- FDA Inspection 1156933 - 2021-10-21
- FDA Inspection 1113269 - 2019-10-17
- FDA Inspection 1106449 - 2019-09-13
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