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FDA Import Refusal 799-6793626-9/11/1 — MeKo Manufacturing E.K.

MeKo Manufacturing E.K. — FEI 3009937642

The FDA refused shipment 799-6793626-9/11/1 from MeKo Manufacturing E.K. (Germany) on May 6, 2020. The refused product falls under Devices — CATHETER, BALLOON TYPE. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
May 6, 2020
Country
Germany
Product Category
Devices
Product Code
79GBA CATHETER, BALLOON TYPE
Charges
118

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Other import refusals

FDA data resources

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