FDA Inspection 1099149 — Resilience US, Inc.

Resilience US, Inc. — FEI 3006316363

The FDA completed an inspection of Resilience US, Inc. on August 9, 2019 in West Chester, OH. 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
August 9, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Chester, OH (United States)