FDA Inspection 1287216 — Kent Elastomer Products Inc

Kent Elastomer Products Inc — FEI 3002303166

The FDA completed an inspection of Kent Elastomer Products Inc on Oct 16, 2025 in Kent, OH. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 16, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Kent, OH (United States)

Citations

IDCFRDescription
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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