# FDA Inspection 680160 - BioIQ - August 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/bioiq/2a5692d2-cfbb-429c-902a-76013a14e925
Source feed: FDA_Inspections

> FDA Inspection 680160 for BioIQ on August 09, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 680160
- Company Name: BioIQ
- Inspection Date: 2010-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 825488 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/bioiq/d8aca6ad-a741-4f11-b90c-11f500ea1d1c)
- [FDA Inspection 825488 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/bioiq/671c096e-3ef9-4b82-92d5-a69ca8ea66a3)

Company: https://www.keypedia.com/companies/bioiq/663d6b8d-baed-4e7a-be78-408890fa4915

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