FDA Import Refusal 799-5010406-5/11/1 — Helioscopie

Helioscopie — FEI 3003323174

The FDA refused shipment 799-5010406-5/11/1 from Helioscopie (France) on Jan 29, 2020. The refused product falls under Devices — IMPLANT, INTRAGASTRIC FOR MORBID OBESITY. Cited charges: 118,237,3280 This firm has 2 other import refusals on record.

Refusal details

Date
Jan 29, 2020
Country
France
Product Category
Devices
Product Code
78LTI IMPLANT, INTRAGASTRIC FOR MORBID OBESITY
Charges
118,237,3280

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