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FDA Import Refusal 581-0198407-7/31/1 — Hilditch Group

Hilditch Group — FEI 3008707923

The FDA refused shipment 581-0198407-7/31/1 from Hilditch Group (United Kingdom) on Apr 2, 2024. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 118,3280,476 This firm has 3 other import refusals on record.

Refusal Details

Date
Apr 2, 2024
Country
United Kingdom
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
118,3280,476

Other import refusals

FDA data resources

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