# FDA Inspection 1206200 - Oricare Inc. - May 03, 2023

Source: https://www.keypedia.com/records/fda_inspections/oricare-inc/b7495ed6-d425-42bd-8f52-4d0dab840fff
Source feed: FDA_Inspections

> FDA Inspection 1206200 for Oricare Inc. on May 03, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1206200
- Company Name: Oricare Inc.
- Inspection Date: 2023-05-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1077604 - 2018-12-11](https://www.keypedia.com/records/fda_inspections/oricare-inc/a4a9f3d8-574a-45ef-8863-5749a9531460)

Company: https://www.keypedia.com/companies/oricare-inc/66a81198-c62a-42fc-bb6c-680c3b71a982

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