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FDA Import Refusal DNA-0341919-3/51/2 — Proctor & Gamble Incorporated

Proctor & Gamble Incorporated — FEI 1000467230

The FDA refused shipment DNA-0341919-3/51/2 from Proctor & Gamble Incorporated (Canada) on Jul 5, 2017. The refused product falls under Devices — PAD, MENSTRUAL, UNSCENTED. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 5, 2017
Country
Canada
Product Category
Devices
Product Code
85HHD PAD, MENSTRUAL, UNSCENTED
Charges
341

Other import refusals

FDA data resources

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