FDA inspection
Sigma-Aldrich Mfg LLC: FDA inspection ending May 12, 2003
FDA inspection 284708 · No Action Indicated (NAI) · Saint Louis, MO
Key facts
| Inspection ID | 284708 |
|---|---|
| Firm | Sigma-Aldrich Mfg LLC |
| FEI number | 1937990 |
| Address | 3300 S 2nd St |
| City | Saint Louis |
| State | MO |
| ZIP | 63118-3306 |
| Fiscal year | 2003 |
| Inspection end date | May 12, 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
- 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