FDA Inspection 1093567 — Zavation

Zavation — FEI 3008583793

The FDA completed an inspection of Zavation on June 20, 2019 in Flowood, MS. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Flowood, MS (United States)

Citations

IDCFRDescription
73221 CFR 803.50(a)(2)Individual Report of Malfunction