# GRI Medical & Electronic Technology Co., Ltd. – FDA Inspection, Sep 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/gri-medical-electronic-technology-co-ltd/e6123713-7ed1-46da-bdd7-8f254f2118a7
Source feed: FDA_Inspections

> FDA inspection 989002 of GRI Medical & Electronic Technology Co., Ltd., September 22, 2016. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989002
- Company Name: GRI Medical & Electronic Technology Co., Ltd.
- Inspection Date: 2016-09-22
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1087779 - 2018-04-19](https://www.keypedia.com/records/fda_inspections/gri-medical-electronic-technology-co-ltd/98c20aef-2e78-41ba-af0d-0a8954388e07)
- FDA Inspection 896201 - 2014-08-14
- [FDA Inspection 813361 - 2012-12-20](https://www.keypedia.com/records/fda_inspections/gri-medical-electronic-technology-co-ltd/f2cbe5ac-5917-4c9d-95b7-d4c4dd7c7a63)

Company: https://www.keypedia.com/companies/gri-medical-electronic-technology-co-ltd/7536a754-5307-4343-8cad-619ddf93d37e

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