# FDA Inspection 1061753 - EMOTECHNIC - May 18, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/emotechnic/590d11d8-ef35-4300-a810-b4045e2860f2
Source feed: FDA_Inspections

> FDA Inspection 1061753 for EMOTECHNIC on May 18, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061753
- Company Name: EMOTECHNIC
- Inspection Date: 2018-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/emotechnic/ac6e7a71-8ddf-41e9-a087-aad2c440d5d7

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