FDA Inspection 675290 - Alive Inc. DBA Hako-Med - August 12, 2010

View on Dashboard

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Copilot

Record Details

This FDA Inspection record concerns Alive Inc. DBA Hako-Med, with an inspection on August 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Alive Inc. DBA Hako-Med
Inspection Date: August 12, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 10b38d03-8016-4988-8dd6-98ebdd5d1f26