FDA Inspection 1260658 — ARCADLAB, LLC

ARCADLAB, LLC — FEI 3014531454

The FDA completed an inspection of ARCADLAB, LLC on Feb 5, 2025 in West Palm 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 5, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Palm Beach, FL (United States)

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