FDA Inspection 1113768 — Red Oak Instruments, LLC

Red Oak Instruments, LLC — FEI 3003786816

The FDA completed an inspection of Red Oak Instruments, LLC on Nov 22, 2019 in Missouri City, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 22, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Missouri City, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.