FDA inspection
Radiation Products Design,Inc: FDA inspection ending Jul 24, 2001
FDA inspection 81168 · Official Action Indicated (OAI) · Albertville, MN
Key facts
| Inspection ID | 81168 |
|---|---|
| Firm | Radiation Products Design,Inc |
| FEI number | 2182762 |
| Address | 5218 Barthel Industrial Dr Ne |
| City | Albertville |
| State | MN |
| ZIP | 55301-9766 |
| Fiscal year | 2001 |
| Inspection end date | Jul 24, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM178570 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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