# Brident Inc – FDA Inspection, Sep 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/brident-inc/f13b33cd-1a83-4175-80cb-24d41d97470d
Source feed: FDA_Inspections

> FDA inspection 943723 of Brident Inc, September 23, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 943723
- Company Name: Brident Inc
- Inspection Date: 2015-09-23
- 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

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