FDA Inspection 1000024 — Artemis Bio-Solutions

Artemis Bio-Solutions — FEI 3009620743

The FDA completed an inspection of Artemis Bio-Solutions on Jan 10, 2017 in Wood Dale, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wood Dale, IL (United States)