FDA inspection
Eurofins Lancaster Laboratories, Inc: FDA inspection ending Jun 18, 2009
FDA inspection 598580 · No Action Indicated (NAI) · Portage, MI
Key facts
| Inspection ID | 598580 |
|---|---|
| Firm | Eurofins Lancaster Laboratories, Inc |
| FEI number | 1833335 |
| Address | 6859 Quality Way |
| City | Portage |
| State | MI |
| ZIP | 49002-9779 |
| Fiscal year | 2009 |
| Inspection end date | Jun 18, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data