Home / Import refusals / 9K9-1006329-3/31/1

FDA Import Refusal 9K9-1006329-3/31/1 — Church & Dwight Inc

Church & Dwight Inc — FEI 2280705

The FDA refused shipment 9K9-1006329-3/31/1 from Church & Dwight Inc (United States) on May 24, 2020. The refused product falls under Devices — KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 24, 2020
Country
United States
Product Category
Devices
Product Code
75LCX KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER
Charges
118,3280,341

Recent inspections

  • 1135841 (NAI Fri Aug 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 937165 (NAI Thu Aug 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 762722 (VAI Mon Feb 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 709138 (OAI Thu Feb 17 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 9X3-0029141-2/90001/1 (Fri Jul 10 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AM1-0230368-3/31/6 (Sat Mar 13 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AM1-0230368-3/31/5 (Sat Mar 13 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AM1-0230368-3/31/7 (Sat Mar 13 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 9K9-1006329-3/21/1 (Sun May 24 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources