# MME Group Inc – FDA Inspection, Aug 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/mme-group-inc/5a64f8df-5b41-4a02-a89f-cb1ac107f4ac
Source feed: FDA_Inspections

> FDA inspection 1102365 of MME Group Inc, August 23, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102365
- Company Name: MME Group Inc
- Inspection Date: 2019-08-23
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/yehualashet-a-gessesse/cb732900-358c-4982-a912-e98fa45142fe)

Company: https://www.keypedia.com/companies/mme-group-inc/08431069-d119-4640-b49a-2349cddedcb7

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