# Michael E. Berend, M.D. – FDA Inspection, Sep 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 of Michael E. Berend, M.D., September 19, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/myra-k-casey/a2fae714-2ba3-4c60-9f54-990fc7b169c9)

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