# FDA Inspection 873183 - Gemore Technology Co., Ltd. - March 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/gemore-technology-co-ltd/e61010b7-ef6e-4bdc-8370-fd106b8e5f8a
Source feed: FDA_Inspections

> FDA Inspection 873183 for Gemore Technology Co., Ltd. on March 20, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 873183
- Company Name: Gemore Technology Co., Ltd.
- Inspection Date: 2014-03-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 984865 - 2016-07-21](https://www.keypedia.com/records/fda_inspections/gemore-technology-co-ltd/45d90cd8-5e26-427a-809e-297d041004cd)
- [FDA Inspection 873183 - 2014-03-20](https://www.keypedia.com/records/fda_inspections/gemore-technology-co-ltd/9b8d2af7-1832-489c-b93d-1e564459a6e9)

Company: https://www.keypedia.com/companies/gemore-technology-co-ltd/48c4d5c8-1950-4b9d-a0be-6e021a9d8331

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