# FDA Inspection 653191 - Braemar Manufacturing, LLC - March 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/braemar-manufacturing-llc/f63d953b-5fb3-4843-a67c-b6ae5c7af5b1
Source feed: FDA_Inspections

> FDA Inspection 653191 for Braemar Manufacturing, LLC on March 24, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 653191
- Company Name: Braemar Manufacturing, LLC
- Inspection Date: 2010-03-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1030857 - 2017-11-02](https://www.keypedia.com/records/fda_inspections/braemar-manufacturing-llc/b31081e8-4291-4bf2-babd-2d9ca597ff01)
- [FDA Inspection 819115 - 2013-02-20](https://www.keypedia.com/records/fda_inspections/braemar-manufacturing-llc/2baeeb58-d00e-46c7-9bc7-b4355035a157)

Company: https://www.keypedia.com/companies/braemar-manufacturing-llc/ee5c6a7c-edac-4a51-b890-5da06890fdf1

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7