FDA inspection
Albion Laboratories, Inc.: FDA inspection ending May 5, 2009
FDA inspection 605779 · Whittemore, IA
Key facts
| Inspection ID | 605779 |
|---|---|
| Firm | Albion Laboratories, Inc. |
| FEI number | 1929996 |
| Address | 515 Broad St |
| City | Whittemore |
| State | IA |
| ZIP | 50598 |
| Fiscal year | 2009 |
| Inspection end date | May 5, 2009 |
| 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