# GD Group USA Co – FDA Inspection, Mar 7, 2014

Source: https://www.keypedia.com/records/fda_inspections/gd-group-usa-co/eb431e4d-8424-4141-909f-c1c2fef0a1fa
Source feed: FDA_Inspections

> FDA inspection 868921 of GD Group USA Co, March 07, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 868921
- Company Name: GD Group USA Co
- Inspection Date: 2014-03-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1115694 - 2020-01-23

Company: https://www.keypedia.com/companies/gd-group-usa-co/4510f42f-05d9-478c-9899-bfb5dae452c7

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