FDA Inspection 1230803 — Digicare Biomedical Technology, Inc.

Digicare Biomedical Technology, Inc. — FEI 3000718682

The FDA completed an inspection of Digicare Biomedical Technology, Inc. on Feb 6, 2024 in Boynton Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 6, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Boynton Beach, FL (United States)