FDA Inspection 893188 — Vero Biotech LLC

Vero Biotech LLC — FEI 3006775576

The FDA completed an inspection of Vero Biotech LLC on Aug 29, 2014 in Cocoa, FL. 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
Aug 29, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Cocoa, FL (United States)

Citations

IDCFRDescription
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
311721 CFR 820.70(i)Software validation for automated processes
367721 CFR 820.30(g)Design validation - software validation not performed
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate