FDA Inspection 1310684 — Digital Diagnostics Inc.

Digital Diagnostics Inc. — FEI 3014579028

The FDA completed an inspection of Digital Diagnostics Inc. on Mar 20, 2026 in Coralville, IA. 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
Mar 20, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Coralville, IA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.