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FDA Import Refusal 799-8193564-6/11/1 — Pentax Corporation

Pentax Corporation — FEI 3003803439

The FDA refused shipment 799-8193564-6/11/1 from Pentax Corporation (Japan) on Dec 19, 2023. The refused product falls under Devices — COLONOSCOPE, GASTRO-UROLOGY. Cited charges: 118,341,508 This firm has 2 other import refusals on record.

Refusal details

Date
Dec 19, 2023
Country
Japan
Product Category
Devices
Product Code
78FDF COLONOSCOPE, GASTRO-UROLOGY
Charges
118,341,508

Other import refusals

FDA data resources

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