FDA Inspection 1261809 — Sewoon Medical Co., Ltd.

Sewoon Medical Co., Ltd. — FEI 3000247987

The FDA completed an inspection of Sewoon Medical Co., Ltd. on Feb 20, 2025 in Cheonan. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Feb 20, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Cheonan (Korea (the Republic of))

Citations

IDCFRDescription
1471521 CFR 820.30(d)Design output - Lack of or inadequate procedures
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation

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