Home / Import refusals / AV3-0052327-9/571/1

FDA Import Refusal AV3-0052327-9/571/1 — Cosway Company, Inc.

Cosway Company, Inc. — FEI 3000205953

The FDA refused shipment AV3-0052327-9/571/1 from Cosway Company, Inc. (United States) on November 24, 2020. The refused product falls under Drugs and Biologics — OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN). Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 24, 2020
Country
United States
Product Category
Drugs and Biologics
Product Code
66PBJ07 OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
Charges
118

Recent inspections

  • 1250780 (NAI Fri Sep 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1224437 (VAI Fri Oct 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1198266 (VAI Fri Feb 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1006683 (VAI Fri Mar 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 840678 (VAI Thu Jul 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AV3-0052578-7/531/1 (Tue Mar 02 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AV3-0052389-9/211/1 (Tue Dec 08 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AV3-0052389-9/141/1 (Tue Dec 08 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AV3-0052327-9/241/1 (Tue Nov 24 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AV3-0052327-9/621/1 (Tue Nov 24 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources