# FDA Inspection 1114262 - Anschel Technology Inc. - December 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/anschel-technology-inc/1dabd0dd-dcf2-4bbb-a022-4c318d2ee295
Source feed: FDA_Inspections

> FDA Inspection 1114262 for Anschel Technology Inc. on December 31, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1114262
- Company Name: Anschel Technology Inc.
- Inspection Date: 2019-12-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/anschel-technology-inc/df5fe7d8-1632-4dcd-97d2-58af44c7e298

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