FDA inspection
Eurofins Lancaster Laboratories, Inc: FDA inspection ending Apr 25, 2012
FDA inspection 778568 · No Action Indicated (NAI) · Portage, MI
Key facts
| Inspection ID | 778568 |
|---|---|
| Firm | Eurofins Lancaster Laboratories, Inc |
| FEI number | 1833335 |
| Address | 6859 Quality Way |
| City | Portage |
| State | MI |
| ZIP | 49002 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Apr 25, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Pre-Approval Eval. of Animal Drugs and Food Additives |
| Product type | Veterinary |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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