FDA Inspection 1159345 — Suture Concepts

Suture Concepts — FEI 3012101526

The FDA completed an inspection of Suture Concepts on Dec 20, 2021 in Beverly, MA. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 20, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Beverly, MA (United States)

Citations

IDCFRDescription
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
326321 CFR 820.250(b)Sampling plans
333121 CFR 820.181DMR - not or inadequately maintained

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