FDA Inspection 1163356 — Meddev Corp

Meddev Corp — FEI 2921577

The FDA completed an inspection of Meddev Corp on February 28, 2022 in Sunnyvale, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
369621 CFR 820.100(b)Documentation
383721 CFR 820.25(b)Training records
405921 CFR 820.22Quality Audits - defined intervals