FDA Inspection 1193530 — Suture Ease, Inc.

Suture Ease, Inc. — FEI 3009956343

The FDA completed an inspection of Suture Ease, Inc. on December 14, 2022 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 14, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)