# FDA Inspection 986133 - Anschel Technology Inc. - August 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/anschel-technology-inc/331bde32-7964-4daa-a843-c1d79216299c
Source feed: FDA_Inspections

> FDA Inspection 986133 for Anschel Technology Inc. on August 16, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986133
- Company Name: Anschel Technology Inc.
- Inspection Date: 2016-08-16
- 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