FDA Inspection 1163356 — Meddev Corp

Meddev Corp — FEI 2921577

The FDA completed an inspection of Meddev Corp on Feb 28, 2022 in Sunnyvale, CA. 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
Feb 28, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: 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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.