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FDA Import Refusal AEK-7070201-0/2/1 — Wise Instruments Manufacturing Co.

Wise Instruments Manufacturing Co. — FEI 3003882399

The FDA refused shipment AEK-7070201-0/2/1 from Wise Instruments Manufacturing Co. (Pakistan) on Dec 13, 2005. The refused product falls under Devices — NEEDLE, PNEUMOPERITONEUM, SPRING LOADED. Cited charge: 479 This firm has 4 other import refusals on record.

Refusal details

Date
Dec 13, 2005
Country
Pakistan
Product Category
Devices
Product Code
78FHO NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
Charges
479

Other import refusals

FDA data resources

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