# FDA Inspection 638179 - Hemodiagnostica, Llc - January 12, 2010

Source: https://www.keypedia.com/records/fda_inspections/hemodiagnostica-llc/4e789670-3fb7-411e-9044-c69234bb4fe8
Source feed: FDA_Inspections

> FDA Inspection 638179 for Hemodiagnostica, Llc on January 12, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 638179
- Company Name: Hemodiagnostica, Llc
- Inspection Date: 2010-01-12
- 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 638179 - 2010-01-12](https://www.keypedia.com/records/fda_inspections/hemodiagnostica-llc/01c56425-272c-4ab8-b16b-b051eced4311)

Company: https://www.keypedia.com/companies/hemodiagnostica-llc/db5750fe-5225-4af8-ad62-e74ac3704a6b

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