FDA Inspection 828655 — Zander Scientific, Inc.

Zander Scientific, Inc. — FEI 3000215008

The FDA completed an inspection of Zander Scientific, Inc. on April 22, 2013 in Vero Beach, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 22, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Vero Beach, FL (United States)

Citations

IDCFRDescription
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures