FDA Inspection
GD Group USA CoGD Group USA Co – FDA Inspection, Mar 7, 2014
Record Details
This FDA Inspection record concerns GD Group USA Co, with an inspection on March 7, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- GD Group USA Co
- Inspection Date
- March 7, 2014
- Product Type
- Devices
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ID · eb431e4d-8424-4141-909f-c1c2fef0a1fa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 868921
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(b)Review and evaluation for investigation
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of GD Group USA Co
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 23, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for GD Group USA Co
- FDA Inspection 1115694 - 2020-01-23
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