# EMG Technology Co., Ltd. – FDA Inspection, Aug 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/emg-technology-co-ltd/572df990-6175-4662-b77e-926f3ca77541
Source feed: FDA_Inspections

> FDA inspection 1024829 of EMG Technology Co., Ltd., August 17, 2017. Classification: No Action Indicated (NAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024829
- Company Name: EMG Technology Co., Ltd.
- Inspection Date: 2017-08-17
- 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

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- [FDA Inspection 902925 - 2014-10-23](https://www.keypedia.com/records/fda_inspections/emg-technology-co-ltd/fca7b6f6-824b-4829-ba57-ade9ec4bcf0f)
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## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/emg-technology-co-ltd/9596766e-bdd7-42c7-b611-46e34e51af91

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