# FDA Inspection 1005203 - DHEF, Inc. - January 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/dhef-inc/67eec78c-f0e5-48d0-a31b-56236af26509
Source feed: FDA_Inspections

> FDA Inspection 1005203 for DHEF, Inc. on January 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005203
- Company Name: DHEF, Inc.
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/dhef-inc/22852419-40d7-47f4-b4fa-65fdcd6d49c5

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