FDA inspection
Braemar Manufacturing, LLC: FDA inspection ending Dec 12, 2019
FDA inspection 1115717 · No Action Indicated (NAI) · San Diego, CA
Key facts
| Inspection ID | 1115717 |
|---|---|
| Firm | Braemar Manufacturing, LLC |
| FEI number | 3003584029 |
| Address | 3890 Murphy Canyon Rd Ste 100 |
| City | San Diego |
| State | CA |
| ZIP | 92128 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Dec 12, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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