FDA Import Refusal 112-2047934-4/2/1 — Laboratoires Arkopharma
The FDA refused shipment 112-2047934-4/2/1 from Laboratoires Arkopharma (France) on May 13, 2011. The refused product falls under Devices — LUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE. Cited charges: 118,3260,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- May 13, 2011
- Country
- France
- Product Category
- Devices
- Product Code
- 85NUC LUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
- Charges
- 118,3260,508