FDA inspection
Insitu Technologies, Inc.: FDA inspection ending Mar 6, 2002
FDA inspection 223754 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 223754 |
|---|---|
| Firm | Insitu Technologies, Inc. |
| FEI number | 3003407487 |
| Address | 539 Phalen Blvd |
| City | Saint Paul |
| State | MN |
| ZIP | 55130-5303 |
| Fiscal year | 2002 |
| Inspection end date | Mar 6, 2002 |
| 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