FDA Inspection
MME Group IncMME Group Inc – FDA Inspection, Aug 23, 2019
Record Details
This FDA Inspection record concerns MME Group Inc, with an inspection on August 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 5a64f8df-5b41-4a02-a89f-cb1ac107f4ac
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1102365
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
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