# FDA Inspection 1030857 - Braemar Manufacturing, LLC - November 02, 2017

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

> FDA Inspection 1030857 for Braemar Manufacturing, LLC on November 02, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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