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

Source: https://www.keypedia.com/records/fda_inspections/alive-inc-dba-hako-med/10b38d03-8016-4988-8dd6-98ebdd5d1f26
Source feed: FDA_Inspections

> FDA Inspection 675290 for Alive Inc. DBA Hako-Med on August 12, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675290
- Company Name: Alive Inc. DBA Hako-Med
- Inspection Date: 2010-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 675290 - 2010-08-12](https://www.keypedia.com/records/fda_inspections/alive-inc-dba-hako-med/76a24f1e-15a7-4985-a5c9-8ae4888305d5)

Company: https://www.keypedia.com/companies/alive-inc-dba-hako-med/7120d952-4dd8-4bb9-914b-2f78abcd92e9

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7