FDA Inspection 1073332 — Indilab, Inc.

Indilab, Inc. — FEI 1450962

The FDA completed an inspection of Indilab, Inc. on November 28, 2018 in Franklin Park, IL. 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
November 28, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Franklin Park, IL (United States)