FDA inspection
Albion Laboratories, Inc.: FDA inspection ending Mar 14, 2012
FDA inspection 772170 · No Action Indicated (NAI) · Whittemore, IA
Key facts
| Inspection ID | 772170 |
|---|---|
| Firm | Albion Laboratories, Inc. |
| FEI number | 1929996 |
| Address | 515 Broad St |
| City | Whittemore |
| State | IA |
| ZIP | 50598 |
| Fiscal year | 2012 |
| Inspection end date | Mar 14, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feeds, and Devices |
| 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