FDA Import Refusal AEK-1390784-3/11/1 — Autochair
The FDA refused shipment AEK-1390784-3/11/1 from Autochair (United Kingdom) on Jul 26, 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
- Jul 26, 2022
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 80FSA LIFT, PATIENT, NON-AC-POWERED
- Charges
- 341