# FDA Inspection 848720 - Hans Biomed Corporation - August 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/hans-biomed-corporation/f5ff34ed-853b-4d2e-9704-bf1950682b20
Source feed: FDA_Inspections

> FDA Inspection 848720 for Hans Biomed Corporation on August 29, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848720
- Company Name: Hans Biomed Corporation
- Inspection Date: 2013-08-29
- 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/hans-biomed-corporation/60abe6f2-149e-4591-8422-7edc574c65a7

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