FDA inspection
CGR Products MN, LLC.: FDA inspection ending Aug 10, 2004
FDA inspection 341574 · No Action Indicated (NAI) · Inver Grove Heights, MN
Key facts
| Inspection ID | 341574 |
|---|---|
| Firm | CGR Products MN, LLC. |
| FEI number | 3004181163 |
| Address | 6288 Claude Way |
| City | Inver Grove Heights |
| State | MN |
| ZIP | 55076-4435 |
| Fiscal year | 2004 |
| Inspection end date | Aug 10, 2004 |
| 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