FDA Inspection 1030581 — Optos, Inc.

Optos, Inc. — FEI 3005744933

The FDA completed an inspection of Optos, Inc. on Oct 20, 2017 in Southborough, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 20, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Southborough, MA (United States)