# FDA Inspection 943723 - Brident Inc - September 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/brident-inc/e1da4775-020d-43ff-bfdd-2f96a613ab7f
Source feed: FDA_Inspections

> FDA Inspection 943723 for Brident Inc on September 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 943723
- Company Name: Brident Inc
- Inspection Date: 2015-09-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 943723 - 2015-09-23](https://www.keypedia.com/records/fda_inspections/brident-inc/f13b33cd-1a83-4175-80cb-24d41d97470d)

Company: https://www.keypedia.com/companies/brident-inc/8dc415dc-fd9f-43c4-81c9-0192ec79e07b

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