Home / Import refusals / AEK-2985248-7/11/1

FDA Import Refusal AEK-2985248-7/11/1 — ACTAVIS

ACTAVIS — FEI 3013213839

The FDA refused shipment AEK-2985248-7/11/1 from ACTAVIS (Bulgaria) on February 27, 2017. The refused product falls under Drugs and Biologics — VALSARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
February 27, 2017
Country
Bulgaria
Product Category
Drugs and Biologics
Product Code
62ODY12 VALSARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

Other import refusals

  • 799-6937884-0/21/1 (Mon Jul 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • FP1-0021113-4/81/1 (Fri Mar 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-6380727-1/1/1 (Mon Jul 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-6380727-1/1/2 (Mon Jul 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-6380727-1/1/3 (Mon Jul 25 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

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