FDA Import Refusal 799-1120108-5/11/1 — RCL TLB C/O WELCH ALLYN LTD.

RCL TLB C/O WELCH ALLYN LTD. — FEI 3014807731

The FDA refused shipment 799-1120108-5/11/1 from RCL TLB C/O WELCH ALLYN LTD. (Netherlands) on Oct 3, 2022. The refused product falls under Devices — SPIROMETER, DIAGNOSTIC. Cited charges: 3280,341

Refusal details

Date
Oct 3, 2022
Country
Netherlands
Product Category
Devices
Product Code
73BZG SPIROMETER, DIAGNOSTIC
Charges
3280,341

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