FDA Inspection 1234358 — Algomedica, Inc.

Algomedica, Inc. — FEI 3013488109

The FDA completed an inspection of Algomedica, Inc. on Mar 28, 2024 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 28, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Sunnyvale, CA (United States)

Citations

IDCFRDescription
366521 CFR 820.20(b)(3)Management representative
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
405921 CFR 820.22Quality Audits - defined intervals

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