# FDA Inspection 1028621 - Jan Bolinder, MD - September 22, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/jan-bolinder-md/c40669ef-6719-4631-b515-7649f3d92491
Source feed: FDA_Inspections

> FDA Inspection 1028621 for Jan Bolinder, MD on September 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028621
- Company Name: Jan Bolinder, MD
- Inspection Date: 2017-09-22
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/jan-bolinder-md/f928c78e-ebae-47c1-a52e-2b6782fd6e02

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