FDA inspection
Morrison Medical Products: FDA inspection ending Sep 10, 2002
FDA inspection 237959 · No Action Indicated (NAI) · Columbus, OH
Key facts
| Inspection ID | 237959 |
|---|---|
| Firm | Morrison Medical Products |
| FEI number | 1523622 |
| Address | 3735 Paragon Dr |
| City | Columbus |
| State | OH |
| ZIP | 43228-9751 |
| Fiscal year | 2002 |
| Inspection end date | Sep 10, 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