FDA Inspection 1158451 — Artifex Solutions LLC

Artifex Solutions LLC — FEI 3011388423

The FDA completed an inspection of Artifex Solutions LLC on December 2, 2021 in San Juan, PR. 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
December 2, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
San Juan, PR (United States)