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FDA Import Refusal SCS-1489408-5/11/1 — Clinical Resolution Laboratory Inc.

Clinical Resolution Laboratory Inc. — FEI 3005727243

The FDA refused shipment SCS-1489408-5/11/1 from Clinical Resolution Laboratory Inc. (United States) on August 20, 2020. The refused product falls under Devices — POWERED MICRONEEDLE DEVICE. Cited charges: 118,508

Refusal Details

Date
August 20, 2020
Country
United States
Product Category
Devices
Product Code
79QAI POWERED MICRONEEDLE DEVICE
Charges
118,508

Recent inspections

  • 1248213 (VAI Mon Aug 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1219464 (OAI Fri Sep 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1051991 (VAI Tue May 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

FDA data resources