FDA Import Refusal 799-7767003-2/11/1 — Diomed Ltd.

Diomed Ltd. — FEI 3013082516

The FDA refused shipment 799-7767003-2/11/1 from Diomed Ltd. (United Kingdom) on Mar 17, 2022. The refused product falls under Devices — SYSTEM, LASER, PHOTODYNAMIC THERAPY. Cited charges: 118,126,237,3280,341

Refusal details

Date
Mar 17, 2022
Country
United Kingdom
Product Category
Devices
Product Code
79MVF SYSTEM, LASER, PHOTODYNAMIC THERAPY
Charges
118,126,237,3280,341

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