# FDA Inspection 1006268 - Peter Beitsch, MD - March 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/peter-beitsch-md/3b27d7ed-2a35-47f7-aba2-9684516263ed
Source feed: FDA_Inspections

> FDA Inspection 1006268 for Peter Beitsch, MD on March 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006268
- Company Name: Peter Beitsch, MD
- Inspection Date: 2017-03-08
- 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/peter-beitsch-md/d616b01a-a690-40dc-ae84-809f138cff68

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