FDA Inspection 1093339 — Integrated Orbital Implants Inc.

Integrated Orbital Implants Inc. — FEI 3009688114

The FDA completed an inspection of Integrated Orbital Implants Inc. on May 9, 2019 in San Diego, 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 9, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)