FDA Inspection 667442 — Commercial Plastics Kenosha LLC

Commercial Plastics Kenosha LLC — FEI 3007617202

The FDA completed an inspection of Commercial Plastics Kenosha LLC on Jun 10, 2010 in Kenosha, WI. 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). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 10, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Kenosha, WI (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
323121 CFR 820.70(i)Documentation of software validation
383721 CFR 820.25(b)Training records
405921 CFR 820.22Quality Audits - defined intervals
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.