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FDA Import Refusal 218-7000241-3/801/1 — Microtek Dominicana, S.A.

Microtek Dominicana, S.A. — FEI 3003094575

The FDA refused shipment 218-7000241-3/801/1 from Microtek Dominicana, S.A. (Dominican Republic) on November 15, 2018. The refused product falls under Devices — VENTILATOR, EMERGENCY, MANUAL (RESUSCITATOR). Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 15, 2018
Country
Dominican Republic
Product Category
Devices
Product Code
73BTM VENTILATOR, EMERGENCY, MANUAL (RESUSCITATOR)
Charges
341

Recent inspections

  • 1036261 (NAI Wed Aug 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 569111 (NAI Thu Jan 29 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 231-1323809-7/11/1 (Tue Feb 11 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 231-1323809-7/11/3 (Tue Feb 11 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 231-1323809-7/11/2 (Tue Feb 11 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • U35-9290353-9/11/1 (Mon Apr 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 413-9030519-6/1/1 (Wed Mar 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources