# FDA Inspection 1000033 - Dr. Robert M. Bersin - February 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/dr-robert-m-bersin/a4bf8cae-e848-40ce-963a-ce99fec779d3
Source feed: FDA_Inspections

> FDA Inspection 1000033 for Dr. Robert M. Bersin on February 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000033
- Company Name: Dr. Robert M. Bersin
- Inspection Date: 2017-02-03
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 926042 - 2015-04-10](https://www.keypedia.com/records/fda_inspections/dr-robert-m-bersin/cb43c204-eb75-44b7-a34d-ba741f21bf93)

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