FDA Import Refusal 799-4562612-2/11/2 — KELLY SA DE CV

KELLY SA DE CV — FEI 3014166827

The FDA refused shipment 799-4562612-2/11/2 from KELLY SA DE CV (Mexico) on Mar 6, 2018. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charges: 118,3280,508

Refusal details

Date
Mar 6, 2018
Country
Mexico
Product Category
Devices
Product Code
73CAF NEBULIZER (DIRECT PATIENT INTERFACE)
Charges
118,3280,508

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