# FDA Inspection 1000384 - Texas Biostetic Instruments - January 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/texas-biostetic-instruments/797939c2-3c6e-45f8-8801-2c611ef52a04
Source feed: FDA_Inspections

> FDA Inspection 1000384 for Texas Biostetic Instruments on January 24, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1000384
- Company Name: Texas Biostetic Instruments
- Inspection Date: 2017-01-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 903644 - 2014-11-18](https://www.keypedia.com/records/fda_inspections/texas-biostetic-instruments/e6b8af6c-0394-4fe9-aa4b-1caec187d1c4)
- [FDA Inspection 903644 - 2014-11-18](https://www.keypedia.com/records/fda_inspections/texas-biostetic-instruments/8dc6982b-49fc-4c72-ab05-f8c2260e88e2)

Company: https://www.keypedia.com/companies/texas-biostetic-instruments/2ddddce0-76a4-4648-b3a7-702b5339ff8c

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