# Braemar Manufacturing, LLC – FDA Inspection, Nov 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/braemar-manufacturing-llc/b31081e8-4291-4bf2-babd-2d9ca597ff01
Source feed: FDA_Inspections

> FDA inspection 1030857 of Braemar Manufacturing, LLC, November 02, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030857
- Company Name: Braemar Manufacturing, LLC
- Inspection Date: 2017-11-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 819115 - 2013-02-20
- FDA Inspection 653191 - 2010-03-24

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kyle-j-mccracken/5085937f-3231-4639-8d84-0e528a954824)

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