# FDA Inspection 813220 - Mogen Instruments - January 03, 2013

Source: https://www.keypedia.com/records/fda_inspections/mogen-instruments/12983e5d-2405-41c0-80d2-430fb5c708c2
Source feed: FDA_Inspections

> FDA Inspection 813220 for Mogen Instruments on January 03, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 813220
- Company Name: Mogen Instruments
- Inspection Date: 2013-01-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 789185 - 2012-07-02](https://www.keypedia.com/records/fda_inspections/mogen-instruments/9ef4bc76-00ae-4b8a-bcb6-1c89eb6d2f75)
- [FDA Inspection 789185 - 2012-07-02](https://www.keypedia.com/records/fda_inspections/mogen-instruments/71a49604-7018-494d-813f-b770afe47abe)

Company: https://www.keypedia.com/companies/mogen-instruments/f432580c-184e-44fa-a5be-69c6edd579fd

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