FDA Inspection 1026690 — Axolotl Biologix, Inc.

Axolotl Biologix, Inc. — FEI 3012345793

The FDA completed an inspection of Axolotl Biologix, Inc. on August 4, 2017 in Flagstaff, 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
August 4, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Flagstaff, AZ (United States)