FDA Inspection 1195570 — Arthomed, LLC.

Arthomed, LLC. — FEI 3007062429

The FDA completed an inspection of Arthomed, LLC. on Jan 25, 2023 in Delray Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Delray Beach, FL (United States)