FDA Inspection 1256854 — Quadric BioMed, LLC

Quadric BioMed, LLC — FEI 3025467473

The FDA completed an inspection of Quadric BioMed, LLC on Dec 16, 2024 in Colorado Springs, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 16, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Colorado Springs, CO (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures