# FDA Inspection 1102480 - Encision Inc. - September 20, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/encision-inc/53a6dc39-bf2b-46ce-bc5f-777d27594d05
Source feed: FDA_Inspections

> FDA Inspection 1102480 for Encision Inc. on September 20, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102480
- Company Name: Encision Inc.
- Inspection Date: 2019-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102480 - 2019-09-20](https://www.globalkeysolutions.net/records/fda_inspections/encision-inc/8acad7cc-7fd1-48b6-a4da-48dd644d3a79)
- [FDA Inspection 947464 - 2015-10-19](https://www.globalkeysolutions.net/records/fda_inspections/encision-inc/e85940cb-9d75-4b15-934c-cb785dda9bd8)
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- [FDA Inspection 809607 - 2012-12-07](https://www.globalkeysolutions.net/records/fda_inspections/encision-inc/ab5ea58c-521c-4e0c-9a08-20176d411fb2)
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Company: https://www.globalkeysolutions.net/companies/encision-inc/fa84ff9e-c141-4cb9-8cb3-f8a95908068b

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