FDA Inspection 1094240 — REBOUND THERAPEUTICS, CORPORATION

REBOUND THERAPEUTICS, CORPORATION — FEI 3013505638

The FDA completed an inspection of REBOUND THERAPEUTICS, CORPORATION on May 16, 2019 in Irvine, 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
May 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)