# FDA Inspection 817929 - ARJOHUNTLEIGH AB - February 07, 2013

Source: https://www.keypedia.com/records/fda_inspections/arjohuntleigh-ab/b2f550ec-e840-454c-a6d2-b9f9f1a597c3
Source feed: FDA_Inspections

> FDA Inspection 817929 for ARJOHUNTLEIGH AB on February 07, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817929
- Company Name: ARJOHUNTLEIGH AB
- Inspection Date: 2013-02-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 817929 - 2013-02-07](https://www.keypedia.com/records/fda_inspections/arjohuntleigh-ab/9efc8760-56d0-4e08-8af8-13e8e7c13b0c)

Company: https://www.keypedia.com/companies/arjohuntleigh-ab/9132963c-0158-45f1-bc2c-5cc59c61f10c

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