FDA Inspection
DC ELEKTRONIK ABDC ELEKTRONIK AB – FDA Inspection, Feb 8, 2017
Record Details
This FDA Inspection record concerns DC ELEKTRONIK AB, with an inspection on February 8, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 1e60bbcb-a2e3-4381-abf7-e151bec5a00c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1018613
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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