# FDA Inspection 1031501 - Steven Messe, MD - November 09, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/steven-messe-md/adad7eef-15c5-4711-b59b-221b78bc391b
Source feed: FDA_Inspections

> FDA Inspection 1031501 for Steven Messe, MD on November 09, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031501
- Company Name: Steven Messe, MD
- Inspection Date: 2017-11-09
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/steven-messe-md/799d1ada-4fed-48c8-8c2e-310bae5903cc

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