FDA Inspection 946134 — Zentech, Inc.

Zentech, Inc. — FEI 3011685188

The FDA completed an inspection of Zentech, Inc. on Oct 23, 2015 in Clearwater, 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
Oct 23, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Clearwater, FL (United States)