FDA Warning Letter — Red Oak Instruments, LLC

Case 692368 — FEI 3003786816

The FDA took a Warning Letter action against Red Oak Instruments, LLC on Feb 21, 2025 (Missouri City, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Red Oak Instruments, LLC
Date
Feb 21, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Missouri City, TX (United States)

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