# FDA Inspection 729590 - Olympus Biotech Corporation - June 15, 2011

Source: https://www.keypedia.com/records/fda_inspections/olympus-biotech-corporation/9ec1f3bb-2166-46d4-807e-2e049a071585
Source feed: FDA_Inspections

> FDA Inspection 729590 for Olympus Biotech Corporation on June 15, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 729590
- Company Name: Olympus Biotech Corporation
- Inspection Date: 2011-06-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 729590 - 2011-06-15](https://www.keypedia.com/records/fda_inspections/olympus-biotech-corporation/37d0a736-1057-49ed-a8cc-72ece533f188)
- [FDA Inspection 592872 - 2009-06-08](https://www.keypedia.com/records/fda_inspections/olympus-biotech-corporation/4a0ff6c9-51ba-4e2e-8374-9af45d35503d)
- [FDA Inspection 592872 - 2009-06-08](https://www.keypedia.com/records/fda_inspections/olympus-biotech-corporation/78c8f742-33a0-4a09-af81-cac74a59dd5a)

Company: https://www.keypedia.com/companies/olympus-biotech-corporation/732b7687-05b3-4630-abd8-c01a636b0a2f

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