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FDA Import Refusal 799-1387156-3/21/1 — STERIPEN

STERIPEN — FEI 3028736844

The FDA refused shipment 799-1387156-3/21/1 from STERIPEN (Switzerland) on Jun 21, 2024. The refused product falls under Devices — PURIFIER, WATER, ULTRAVIOLET, MEDICAL. Cited charges: 118,3280,341

Refusal Details

Date
Jun 21, 2024
Country
Switzerland
Product Category
Devices
Product Code
80KMG PURIFIER, WATER, ULTRAVIOLET, MEDICAL
Charges
118,3280,341

FDA data resources

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