# FDA Inspection 1073015 - Margaret Dillon - November 02, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/margaret-dillon/015629dc-fe62-463e-b72f-35aa3304c5b7
Source feed: FDA_Inspections

> FDA Inspection 1073015 for Margaret Dillon on November 02, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073015
- Company Name: Margaret Dillon
- Inspection Date: 2018-11-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/margaret-dillon/5c099a9d-62aa-44d2-be80-e86f244cf7e5

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