# FDA Inspection 631013 - Encision Inc. - December 02, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/encision-inc/a1cb94d5-051b-4f7d-aa89-2706ddbf8005
Source feed: FDA_Inspections

> FDA Inspection 631013 for Encision Inc. on December 02, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 631013
- Company Name: Encision Inc.
- Inspection Date: 2009-12-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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