FDA Import Refusal 9H5-0010019-7/11/1 — KONICA MINOLTA HEALTHCARE DO BRA

KONICA MINOLTA HEALTHCARE DO BRA — FEI 3026586774

The FDA refused shipment 9H5-0010019-7/11/1 from KONICA MINOLTA HEALTHCARE DO BRA (Brazil) on Apr 14, 2023. The refused product falls under Devices — SYSTEM, X-RAY, STATIONARY. Cited charge: 118

Refusal details

Date
Apr 14, 2023
Country
Brazil
Product Category
Devices
Product Code
90KPR SYSTEM, X-RAY, STATIONARY
Charges
118

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