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FDA Import Refusal E8L-1005779-7/1/1 — Pentax of America Inc

Pentax of America Inc — FEI 1000080301

The FDA refused shipment E8L-1005779-7/1/1 from Pentax of America Inc (United States) on June 10, 2009. The refused product falls under Devices — ENDOSCOPE, AC-POWERED AND ACCESSORIES. Cited charge: 341 This firm has 3 other import refusals on record.

Refusal Details

Date
June 10, 2009
Country
United States
Product Category
Devices
Product Code
78GCP ENDOSCOPE, AC-POWERED AND ACCESSORIES
Charges
341

Recent inspections

  • 1211451 (NAI Thu Jul 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066901 (VAI Thu Sep 27 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 921077 (OAI Thu Apr 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906155 (VAI Wed Dec 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 812553 (OAI Tue Dec 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 799-6436376-7/11/1 (Wed Mar 05 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • E84-0058192-0/1/1 (Tue Nov 25 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • E84-0058192-0/1/2 (Tue Nov 25 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources