# FDA Inspection 1032333 - FEELTECH CO., LTD. - November 08, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/feeltech-co-ltd/f8dd23d8-3ed7-4b5a-a2a6-30b8fb54dfeb/
Source feed: FDA_Inspections

> FDA Inspection 1032333 for FEELTECH CO., LTD. on November 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032333
- Company Name: FEELTECH CO., LTD.
- Inspection Date: 2017-11-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/feeltech-co-ltd/24f31825-dc84-4d7a-ba35-bb00b292d14b

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