FDA Inspection 1057282 — Polyzen, Inc.

Polyzen, Inc. — FEI 3002897588

The FDA completed an inspection of Polyzen, Inc. on Mar 15, 2018 in Apex, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Apex, NC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.