# Braemar Manufacturing, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/braemar-manufacturing-llc/18f44208-c4bc-411f-9c75-2b852b78fa02

> Inspection records and compliance data for Braemar Manufacturing, LLC in San Diego, California. Access full analysis and detailed observations.

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## Details

- Name: Braemar Manufacturing, LLC
- FEI Number: 3003584029
- City: San Diego
- State: California
- Country Name: United States
- Address Line 1: 3890 Murphy Canyon Rd Ste 100
- Zip Code: 92123

## Related Documents

- [FDA Inspection 1260040 - Braemar Manufacturing, LLC - 2025-01-10](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/e6acda7b-7eb3-4baf-8479-aecb0fec5b73) — source: FDA, date: January 10, 2025
- [FDA Inspection 1260040 - Braemar Manufacturing, LLC - 2025-01-10](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/2877e726-8a83-4d33-8bd5-699b131decc5) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2025
- [FDA Inspection 1260040 - Braemar Manufacturing, LLC - 2025-01-10](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/52824dc2-eb92-44c6-b572-96be40af96b5) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2025
- [FDA Inspection 1115717 - Braemar Manufacturing, LLC - 2019-12-12](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/ccb88b9e-cfef-4340-90bd-5a5f6b5c16c4) — classification: No Action Indicated (NAI), source: FDA, date: December 12, 2019
- [FDA Inspection 760437 - Braemar Manufacturing, LLC - 2011-12-20](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/dd525a85-f94e-4eaf-a8c9-163f1d708684) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2011
- [FDA Inspection 760437 - Braemar Manufacturing, LLC - 2011-12-20](https://www.globalkeysolutions.net/records/fda_inspections/braemar-manufacturing-llc/ba8d91f8-bd61-403b-a64d-16e43815ad8a) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2011

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