# Kyocera Medical Technologies, Inc – FDA Inspection, Feb 4, 2016

Source: https://www.keypedia.com/records/fda_inspections/kyocera-medical-technologies-inc/ee455da1-5d8b-4867-858e-df57096afb6c
Source feed: FDA_Inspections

> FDA inspection 956387 of Kyocera Medical Technologies, Inc, February 04, 2016. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 956387
- Company Name: Kyocera Medical Technologies, Inc
- Inspection Date: 2016-02-04
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1151279 - 2021-08-19
- [FDA Inspection 915196 - 2015-02-13](https://www.keypedia.com/records/fda_inspections/kyocera-medical-technologies-inc/373edc18-43e4-475f-8020-4a6b564230b6)
- FDA Inspection 769505 - 2012-02-09

Company: https://www.keypedia.com/companies/kyocera-medical-technologies-inc/d2110473-c6d2-45a6-b06b-8e181931e597

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