FDA Inspection 1262635 — Reliance Dental Manufacturing LLC

Reliance Dental Manufacturing LLC — FEI 1415367

The FDA completed an inspection of Reliance Dental Manufacturing LLC on Mar 4, 2025 in Alsip, IL. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 4, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Alsip, IL (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
54621 CFR 820.75(a)Lack of or inadequate process validation

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