FDA Inspection
JAMM Technologies IncJAMM Technologies Inc – FDA Inspection, Jan 17, 2018
Record Details
This FDA Inspection record concerns JAMM Technologies Inc, with an inspection on January 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 42080d48-c113-468a-8264-4040da8dd127
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1038911
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.30(d)Design output - documentation
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
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