# FDA Inspection 1021125 - Subhash Banerjee - June 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/subhash-banerjee/1b728d44-0135-4f62-9061-969c51783a27
Source feed: FDA_Inspections

> FDA Inspection 1021125 for Subhash Banerjee on June 23, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021125
- Company Name: Subhash Banerjee
- Inspection Date: 2017-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/subhash-banerjee/7d45e883-48d8-4fde-8350-a2c3b7953b4c

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