# FDA Inspection 1008837 - MAI/GENESIS - April 05, 2017

Source: https://www.keypedia.com/records/fda_inspections/maigenesis/b086d801-589a-41cf-aa19-029297da6ed6
Source feed: FDA_Inspections

> FDA Inspection 1008837 for MAI/GENESIS on April 05, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008837
- Company Name: MAI/GENESIS
- Inspection Date: 2017-04-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/maigenesis/daf3e45e-383f-431c-8026-26dddc1bfa8f

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