# FDA Inspection 947895 - Gerard Reilly MD - November 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/gerard-reilly-md/803d09a3-90b3-49b9-80ff-1436dde40b92
Source feed: FDA_Inspections

> FDA Inspection 947895 for Gerard Reilly MD on November 16, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 947895
- Company Name: Gerard Reilly MD
- Inspection Date: 2015-11-16
- 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/gerard-reilly-md/a89b0ae2-6eed-49a5-91bb-8f72af657bb2

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