# DGH Technology Inc – FDA Inspection, Aug 3, 2016

Source: https://www.keypedia.com/records/fda_inspections/dgh-technology-inc/a89f3ebd-7025-416c-be53-8cfdfa483f68
Source feed: FDA_Inspections

> FDA inspection 983608 of DGH Technology Inc, August 03, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983608
- Company Name: DGH Technology Inc
- Inspection Date: 2016-08-03
- 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: 3

## Related Documents

- FDA Inspection 1257099 - 2024-11-22
- FDA Inspection 856329 - 2013-11-22
- FDA Inspection 703143 - 2010-12-22

Company: https://www.keypedia.com/companies/dgh-technology-inc/892ccfaa-4fd4-49e9-95aa-28bec8cfb02a

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