# FDA Inspection 926042 - Dr. Robert M. Bersin - April 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/dr-robert-m-bersin/cb43c204-eb75-44b7-a34d-ba741f21bf93
Source feed: FDA_Inspections

> FDA Inspection 926042 for Dr. Robert M. Bersin on April 10, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926042
- Company Name: Dr. Robert M. Bersin
- Inspection Date: 2015-04-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1000033 - 2017-02-03](https://www.keypedia.com/records/fda_inspections/dr-robert-m-bersin/a4bf8cae-e848-40ce-963a-ce99fec779d3)

Company: https://www.keypedia.com/companies/dr-robert-m-bersin/dc34ba20-1cd5-42f3-993a-1031e657b701

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