# FDA Inspection 805918 - Electronique du Mazet - October 18, 2012

Source: https://www.keypedia.com/records/fda_inspections/electronique-du-mazet/2ddf6dec-93e2-4433-bfc6-b8d8e19c2d93
Source feed: FDA_Inspections

> FDA Inspection 805918 for Electronique du Mazet on October 18, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805918
- Company Name: Electronique du Mazet
- Inspection Date: 2012-10-18
- 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/electronique-du-mazet/7d5ffee4-e1b3-4401-8d40-4e50f17a9d0b

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