FDA Inspection
DGH Technology IncDGH Technology Inc – FDA Inspection, Aug 3, 2016
Record Details
This FDA Inspection record concerns DGH Technology Inc, with an inspection on August 3, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DGH Technology Inc
- Inspection Date
- August 3, 2016
- Product Type
- Devices
View Company Profile
ID · a89f3ebd-7025-416c-be53-8cfdfa483f68
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 983608
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.70(b)Production and Process Change Procedures, lack of or Inad.
- 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 DGH Technology Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 22, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 22, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 22, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for DGH Technology Inc
- FDA Inspection 1257099 - 2024-11-22
- FDA Inspection 856329 - 2013-11-22
- FDA Inspection 703143 - 2010-12-22
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