FDA Inspection 954582 — ADVAN INT'L CORP KOREA BRANCH

ADVAN INT'L CORP KOREA BRANCH — FEI 3009925724

The FDA completed an inspection of ADVAN INT'L CORP KOREA BRANCH on Nov 10, 2015 in Yeouido-dong Yeongdeungpo-gu Seoul. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 10, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Yeouido-dong Yeongdeungpo-gu Seoul (Korea (the Republic of))

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
326321 CFR 820.250(b)Sampling plans

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