# FDA Inspection 1037621 - Bruin Manufacturing Company, Inc. - January 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/bruin-manufacturing-company-inc/2081b5ec-08d5-4288-b6a4-e4e59011158c
Source feed: FDA_Inspections

> FDA Inspection 1037621 for Bruin Manufacturing Company, Inc. on January 12, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037621
- Company Name: Bruin Manufacturing Company, Inc.
- Inspection Date: 2018-01-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 904385 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/bruin-manufacturing-company-inc/7abc2e68-483e-4965-bb52-c32e7710406d)
- [FDA Inspection 904385 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/bruin-manufacturing-company-inc/a1b6aff6-1356-478d-b19c-a14bd30c08a4)

Company: https://www.keypedia.com/companies/bruin-manufacturing-company-inc/4c5fd544-2502-4c91-8676-d993ad5f57fa

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