# Mogen Instruments – FDA Inspection, Jul 2, 2012

Source: https://www.keypedia.com/records/fda_inspections/mogen-instruments/9ef4bc76-00ae-4b8a-bcb6-1c89eb6d2f75
Source feed: FDA_Inspections

> FDA inspection 789185 of Mogen Instruments, July 02, 2012. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 789185
- Company Name: Mogen Instruments
- Inspection Date: 2012-07-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 813220 - 2013-01-03

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