FDA inspection
Caleb Laboratories: FDA inspection ending Jan 11, 2000
FDA inspection 9520 · Official Action Indicated (OAI) · Minneapolis, MN
Key facts
| Inspection ID | 9520 |
|---|---|
| Firm | Caleb Laboratories |
| FEI number | 2127066 |
| Address | 529 S 7th St Ste 288 |
| City | Minneapolis |
| State | MN |
| ZIP | 55415-1897 |
| Fiscal year | 2000 |
| Inspection end date | Jan 11, 2000 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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