# Oak Ridge Products – FDA Inspection, Sep 30, 2022

Source: https://www.keypedia.com/records/fda_inspections/oak-ridge-products/65a5c1d6-8d2f-47f2-8abd-052dafefd15a
Source feed: FDA_Inspections

> FDA inspection 1180761 of Oak Ridge Products, September 30, 2022. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1180761
- Company Name: Oak Ridge Products
- Inspection Date: 2022-09-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1310976 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/oak-ridge-products/cd10db90-8327-4e3f-ad14-2bcd2e616c19)
- [FDA Inspection 1029908 - 2017-10-26](https://www.keypedia.com/records/fda_inspections/oak-ridge-products/98904bff-0431-499a-a51d-9b843df07bdf)

Company: https://www.keypedia.com/companies/oak-ridge-products/3beacb33-dcdb-4d02-9cd1-84e72e19ae97

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