# FDA Inspection 1080165 - Kenneth Snyder, M.D. - February 13, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kenneth-snyder-md/4aa11488-a28f-4ade-87e1-80ca930895d4
Source feed: FDA_Inspections

> FDA Inspection 1080165 for Kenneth Snyder, M.D. on February 13, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1080165
- Company Name: Kenneth Snyder, M.D.
- Inspection Date: 2019-02-13
- 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/kenneth-snyder-md/d65c6a32-57bb-4bf7-a72c-d50bda43ccdc

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