FDA Inspection 1081409 — Arthomed, LLC.

Arthomed, LLC. — FEI 3007062429

The FDA completed an inspection of Arthomed, LLC. on Feb 22, 2019 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
Feb 22, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Delray Beach, FL (United States)