# FDA Inspection 1026777 - Cesar Keller, MD - August 21, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/cesar-keller-md/dbde1e95-24cf-4576-b826-3cd2c259ebe7
Source feed: FDA_Inspections

> FDA Inspection 1026777 for Cesar Keller, MD on August 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026777
- Company Name: Cesar Keller, MD
- Inspection Date: 2017-08-21
- 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/cesar-keller-md/cad2a801-f849-4091-b738-0383dbc90b27

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