FDA Inspection 1250756 — CryoFuture, Inc.

CryoFuture, Inc. — FEI 3023823559

The FDA completed an inspection of CryoFuture, Inc. on Sep 19, 2024 in San Mateo, CA. 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
Sep 19, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Mateo, CA (United States)