FDA inspection
Amico Laboratories Inc: FDA inspection ending Jan 30, 2003
FDA inspection 255200 · No Action Indicated (NAI) · Nashville, TN
Key facts
| Inspection ID | 255200 |
|---|---|
| Firm | Amico Laboratories Inc |
| FEI number | 1034157 |
| Address | 5012 Illinois Ave |
| City | Nashville |
| State | TN |
| ZIP | 37209-2108 |
| Fiscal year | 2003 |
| Inspection end date | Jan 30, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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