# FDA Inspection 795620 - Sekisui Diagnostics, LLC - August 14, 2012

Source: https://www.keypedia.com/records/fda_inspections/sekisui-diagnostics-llc/83f03cbb-7e17-4529-bba8-da05edbcc284
Source feed: FDA_Inspections

> FDA Inspection 795620 for Sekisui Diagnostics, LLC on August 14, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 795620
- Company Name: Sekisui Diagnostics, LLC
- Inspection Date: 2012-08-14
- 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 1113282 - 2019-12-10](https://www.keypedia.com/records/fda_inspections/sekisui-diagnostics-llc/bc231361-c98e-4e20-bff6-e2ed3801fe68)
- [FDA Inspection 1113282 - 2019-12-10](https://www.keypedia.com/records/fda_inspections/sekisui-diagnostics-llc/e9ab2a37-7286-468e-b392-ea8f107f8da4)
- [FDA Inspection 795620 - 2012-08-14](https://www.keypedia.com/records/fda_inspections/sekisui-diagnostics-llc/ad5922ed-2e7b-40f0-ac57-aeb2906b8bd6)

Company: https://www.keypedia.com/companies/sekisui-diagnostics-llc/ed661c03-e1cc-4578-ad5a-f68f718bd659

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