FDA Inspection 1042762 — Serim Research Corporation

Serim Research Corporation — FEI 1833387

The FDA completed an inspection of Serim Research Corporation on Feb 23, 2018 in Elkhart, IN. 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
Feb 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkhart, IN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
317221 CFR 820.198(c)Investigation of device failures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ

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