# FDA Inspection 821895 - Hema Diagnostic Systems, L.L.C. - March 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/hema-diagnostic-systems-llc/3651201c-7a10-4c6a-a409-c0195d4db2cd
Source feed: FDA_Inspections

> FDA Inspection 821895 for Hema Diagnostic Systems, L.L.C. on March 11, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821895
- Company Name: Hema Diagnostic Systems, L.L.C.
- Inspection Date: 2013-03-11
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 909107 - 2014-12-10](https://www.keypedia.com/records/fda_inspections/hema-diagnostic-systems-llc/597c5268-4965-4ff7-b0c3-dc49d6123f74)
- [FDA Inspection 909107 - 2014-12-10](https://www.keypedia.com/records/fda_inspections/hema-diagnostic-systems-llc/2b69a279-564a-4726-895b-d38ca4cc8b53)
- [FDA Inspection 821895 - 2013-03-11](https://www.keypedia.com/records/fda_inspections/hema-diagnostic-systems-llc/a7bd7e3b-27dc-4fc2-8b5b-88a79576481b)

Company: https://www.keypedia.com/companies/hema-diagnostic-systems-llc/2dbaa05c-2b34-41b8-81b8-e6537a997a37

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