FDA inspection
Braemar Manufacturing, LLC: FDA inspection ending Apr 28, 2006
FDA inspection 425823 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 425823 |
|---|---|
| Firm | Braemar Manufacturing, LLC |
| FEI number | 3003584029 |
| Address | 3890 Murphy Canyon Rd Ste 100 |
| City | San Diego |
| State | CA |
| ZIP | 92123-4448 |
| Fiscal year | 2006 |
| Inspection end date | Apr 28, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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