# FDA Inspection 1101933 - Bergen Medical Products, Inc. - September 11, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/bergen-medical-products-inc/b73014d3-3337-4b94-82bd-f879ff605903
Source feed: FDA_Inspections

> FDA Inspection 1101933 for Bergen Medical Products, Inc. on September 11, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101933
- Company Name: Bergen Medical Products, Inc.
- Inspection Date: 2019-09-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101933 - 2019-09-11](https://www.globalkeysolutions.net/records/fda_inspections/bergen-medical-products-inc/90591468-6dce-4a4b-93e1-0820995a35db)

Company: https://www.globalkeysolutions.net/companies/bergen-medical-products-inc/cbe907b7-c4ef-481a-bd44-a134f9bf8bf9

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