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FDA Import Refusal 799-3629836-1/11/1 — KMI/IMI Group

KMI/IMI Group — FEI 3015763642

The FDA refused shipment 799-3629836-1/11/1 from KMI/IMI Group (United Kingdom) on Sep 23, 2019. The refused product falls under Devices — UNIT, ELECTROLYSIS, BATTERY-POWERED, OPHTHALMIC. Cited charges: 118,3280

Refusal details

Date
Sep 23, 2019
Country
United Kingdom
Product Category
Devices
Product Code
86HPY UNIT, ELECTROLYSIS, BATTERY-POWERED, OPHTHALMIC
Charges
118,3280

FDA data resources

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