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FDA Inspection 1087896 — Matthew Caldwell, MD

Matthew Caldwell, MD — FEI 3015210223

The FDA completed an inspection of Matthew Caldwell, MD on April 10, 2019 in Lackland Afb, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 10, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lackland Afb, TX (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources