FDA Inspection 1061621 — TissueTech, Inc.

TissueTech, Inc. — FEI 3006717666

The FDA completed an inspection of TissueTech, Inc. on Jul 26, 2018 in San Diego, 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
Jul 26, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Diego, CA (United States)