# FDA Inspection 1025827 - Michael E. Berend, M.D. - September 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/michael-e-berend-md/a85e27ab-66e1-4387-ac0b-6b829cf63518
Source feed: FDA_Inspections

> FDA Inspection 1025827 for Michael E. Berend, M.D. on September 19, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025827
- Company Name: Michael E. Berend, M.D.
- Inspection Date: 2017-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/michael-e-berend-md/a79d5357-2ffa-4d12-bdf0-03ccedc5a636

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