FDA Inspection 1252012 — Biomerics IMP Mebane LLC

Biomerics IMP Mebane LLC — FEI 1000140478

The FDA completed an inspection of Biomerics IMP Mebane LLC on Oct 18, 2024 in Mebane, NC. 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 18, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Mebane, NC (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
369621 CFR 820.100(b)Documentation

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