FDA Import Refusal 799-9531624-2/21/1 — HEMOFARM PROIZVODNJA FARMACEUTSK

HEMOFARM PROIZVODNJA FARMACEUTSK — FEI 3013265840

The FDA refused shipment 799-9531624-2/21/1 from HEMOFARM PROIZVODNJA FARMACEUTSK (Bosnia and Herzegovina) on Mar 16, 2017. The refused product falls under Drugs and Biologics — SILDENAFIL CITRATE (REGULATOR). Cited charge: 75

Refusal details

Date
Mar 16, 2017
Country
Bosnia and Herzegovina
Product Category
Drugs and Biologics
Product Code
65PCA02 SILDENAFIL CITRATE (REGULATOR)
Charges
75

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.