FDA Import Refusal 110-0323968-2/1/1 — Skylark Device & System Co Ltd

Skylark Device & System Co Ltd — FEI 3003040024

The FDA refused shipment 110-0323968-2/1/1 from Skylark Device & System Co Ltd (Taiwan) on Mar 23, 2005. The refused product falls under Devices — STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF. Cited charge: 508

Refusal details

Date
Mar 23, 2005
Country
Taiwan
Product Category
Devices
Product Code
84GZJ STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF
Charges
508

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