# FDA Inspection 1087896 - Matthew Caldwell, MD - April 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/matthew-caldwell-md/3e5d50c7-9bce-4d90-b7e5-df54831d717c
Source feed: FDA_Inspections

> FDA Inspection 1087896 for Matthew Caldwell, MD on April 10, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087896
- Company Name: Matthew Caldwell, MD
- Inspection Date: 2019-04-10
- 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/matthew-caldwell-md/82b87416-97db-4abd-9cf9-3404d2001b8e

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