# FDA Inspection 1021256 - Mark B. Anderson, MD - August 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/mark-b-anderson-md/b980d73a-534f-486e-87be-7ce6a176859d
Source feed: FDA_Inspections

> FDA Inspection 1021256 for Mark B. Anderson, MD on August 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021256
- Company Name: Mark B. Anderson, MD
- Inspection Date: 2017-08-03
- 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/mark-b-anderson-md/ba29e38b-ad68-4b6a-b08a-0f1c95e08211

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