FDA Inspection 1028826 — Entrotech Life Sciences, Inc.

Entrotech Life Sciences, Inc. — FEI 3011393407

The FDA completed an inspection of Entrotech Life Sciences, Inc. on Oct 4, 2017 in Columbus, OH. 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
Oct 4, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)