# DJO, LLC – FDA Inspection, Sep 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/djo-llc/cba7d30a-a173-42f4-ad01-e468321478d5
Source feed: FDA_Inspections

> FDA inspection 848742 of DJO, LLC, September 06, 2013. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 848742
- Company Name: DJO, LLC
- Inspection Date: 2013-09-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1028587 - 2017-09-26](https://www.keypedia.com/records/fda_inspections/djo-llc/57dbc0de-ae9f-43bf-a325-8268a7b07640)
- [FDA Inspection 1028586 - 2017-09-26](https://www.keypedia.com/records/fda_inspections/djo-llc/1c65dd21-e33d-4caa-857b-b35bbd620001)
- [FDA Inspection 735208 - 2011-07-14](https://www.keypedia.com/records/fda_inspections/djo-llc/f91b5f9d-dd44-4419-b8fb-d69dbbb8be4e)

Company: https://www.keypedia.com/companies/djo-llc/39fd7e1c-f887-44dc-be4d-0c0d02763842

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