FDA Import Refusal AEK-1270658-4/11/1 — Autochair

Autochair — FEI 3008926093

The FDA refused shipment AEK-1270658-4/11/1 from Autochair (United Kingdom) on Jun 17, 2022. The refused product falls under Devices — LIFT, PATIENT, NON-AC-POWERED. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 17, 2022
Country
United Kingdom
Product Category
Devices
Product Code
80FSA LIFT, PATIENT, NON-AC-POWERED
Charges
341

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