FDA inspection
Braemar Manufacturing, LLC: FDA inspection ending Jan 10, 2012
FDA inspection 794011 · San Diego, CA
Key facts
| Inspection ID | 794011 |
|---|---|
| Firm | Braemar Manufacturing, LLC |
| FEI number | 3003584029 |
| Address | 3890 Murphy Canyon Rd Ste 100 |
| City | San Diego |
| State | CA |
| ZIP | 92123-4448 |
| Fiscal year | 2012 |
| Inspection end date | Jan 10, 2012 |
| 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