FDA Import Refusal AEK-2985248-7/11/1 — ACTAVIS
The FDA refused shipment AEK-2985248-7/11/1 from ACTAVIS (Bulgaria) on Feb 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
- Feb 27, 2017
- Country
- Bulgaria
- Product Category
- Drugs and Biologics
- Product Code
- 62ODY12 VALSARTAN (ANTI-HYPERTENSIVE - PART II)
- Charges
- 75