FDA Inspection 1000569 — Alphacord, LLC

Alphacord, LLC — FEI 3005810197

The FDA completed an inspection of Alphacord, LLC on February 10, 2017 in Scottsdale, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 10, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Scottsdale, AZ (United States)