FDA Inspection 1001617 — ARCH Medical Solutions - Elmhurst

ARCH Medical Solutions - Elmhurst — FEI 3002795782

The FDA completed an inspection of ARCH Medical Solutions - Elmhurst on Nov 22, 2016 in Elmhurst, 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
Nov 22, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Elmhurst, IL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements

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