# FDA Inspection 913796 - Titertek Instruments Inc - February 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/titertek-instruments-inc/7dd5c55b-8a3b-41da-a67f-86fe5f030423
Source feed: FDA_Inspections

> FDA Inspection 913796 for Titertek Instruments Inc on February 10, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 913796
- Company Name: Titertek Instruments Inc
- Inspection Date: 2015-02-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 762732 - 2012-01-12](https://www.keypedia.com/records/fda_inspections/titertek-instruments-inc/9155929d-68c3-4c46-bab9-e90a4c125167)
- [FDA Inspection 762732 - 2012-01-12](https://www.keypedia.com/records/fda_inspections/titertek-instruments-inc/4eaa80ed-81e5-4c88-8778-7bc49ae128b6)

Company: https://www.keypedia.com/companies/titertek-instruments-inc/fdfec7b8-613c-4381-bb94-f34ca939b95b

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