# FDA Inspection 1020263 - Patrick Slater, MD - July 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/patrick-slater-md/1c123b2e-2e0e-4139-9857-4b76ca5363b2
Source feed: FDA_Inspections

> FDA Inspection 1020263 for Patrick Slater, MD on July 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020263
- Company Name: Patrick Slater, MD
- Inspection Date: 2017-07-14
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/patrick-slater-md/05a2c388-5e72-4e53-81e9-2a9a8cee9951

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