# FDA Inspection 981333 - Moog Medical Devices Group - July 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/moog-medical-devices-group/560762ab-975f-4336-b8d6-19b5b1cc0858
Source feed: FDA_Inspections

> FDA Inspection 981333 for Moog Medical Devices Group on July 07, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981333
- Company Name: Moog Medical Devices Group
- Inspection Date: 2016-07-07
- 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/moog-medical-devices-group/a5f63678-302b-4583-ba95-fd11dc475afc

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