FDA Import Refusal 799-1532737-0/11/1 — Microlife Ag

Microlife Ag — FEI 3006163325

The FDA refused shipment 799-1532737-0/11/1 from Microlife Ag (Switzerland) on Aug 30, 2017. The refused product falls under Devices — SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Aug 30, 2017
Country
Switzerland
Product Category
Devices
Product Code
74DXN SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
Charges
118

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