FDA Import Refusal AEK-0514676-3/1/1 — Stoddard Mfg. Co. Ltd.

Stoddard Mfg. Co. Ltd. — FEI 3006174523

The FDA refused shipment AEK-0514676-3/1/1 from Stoddard Mfg. Co. Ltd. (United Kingdom) on Jan 21, 2015. The refused product falls under Devices — CUP, PROPHYLAXIS. Cited charge: 341 This firm has 1 other import refusal on record.

Refusal details

Date
Jan 21, 2015
Country
United Kingdom
Product Category
Devices
Product Code
76EHK CUP, PROPHYLAXIS
Charges
341

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