FDA inspection
Braemar Manufacturing, LLC: FDA inspection ending Oct 27, 2003
FDA inspection 300755 · No Action Indicated (NAI) · Eagan, MN
Key facts
| Inspection ID | 300755 |
|---|---|
| Firm | Braemar Manufacturing, LLC |
| FEI number | 1000520785 |
| Address | 1285 Corporate Center Dr Ste 150 |
| City | Eagan |
| State | MN |
| ZIP | 55121-1278 |
| Fiscal year | 2004 |
| Inspection end date | Oct 27, 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
- 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