# FDA Inspection 636028 - Arjohuntleigh Magog, Inc. - October 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/arjohuntleigh-magog-inc/cb8e5874-a6e1-4c25-b949-756d229fdcca
Source feed: FDA_Inspections

> FDA Inspection 636028 for Arjohuntleigh Magog, Inc. on October 29, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 636028
- Company Name: Arjohuntleigh Magog, Inc.
- Inspection Date: 2009-10-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 636028 - 2009-10-29](https://www.keypedia.com/records/fda_inspections/arjohuntleigh-magog-inc/54bac212-f0be-4f91-92c2-af7d66a3d9d7)

Company: https://www.keypedia.com/companies/arjohuntleigh-magog-inc/2ded51a6-30fa-4144-b7a9-1e37566bf9f4

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