Home / Import refusals / 799-8158859-5/10001/1

FDA Import Refusal 799-8158859-5/10001/1 — Anika Therapeutics, Inc.

Anika Therapeutics, Inc. — FEI 3007093114

The FDA refused shipment 799-8158859-5/10001/1 from Anika Therapeutics, Inc. (United States) on November 21, 2025. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 21, 2025
Country
United States
Product Category
Devices
Product Code
87MOZ ACID, HYALURONIC, INTRAARTICULAR
Charges
118,341

Recent inspections

  • 1305600 (NAI Mon Apr 13 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1281778 (VAI Thu Jan 22 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1214830 (VAI Wed Aug 09 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025975 (VAI Thu Sep 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934403 (NAI Fri May 22 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-8170579-8/11/1 (Mon Jan 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-9441785-7/11/1 (Fri Aug 18 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • H77-0210295-2/11/2 (Wed May 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • H77-0210295-2/11/3 (Wed May 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • H77-0210226-7/11/1 (Wed Apr 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources