# FDA Inspection 1001756 - Teksmart Fitness LLC - February 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/c1c29934-3d33-47e6-8bac-bda8e9c1d208
Source feed: FDA_Inspections

> FDA Inspection 1001756 for Teksmart Fitness LLC on February 15, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001756
- Company Name: Teksmart Fitness LLC
- Inspection Date: 2017-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 774747 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/0c55aae9-8c42-40e5-b572-4b013929676a)
- [FDA Inspection 774747 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/71763639-529d-4e89-8837-d5b226def1cb)
- [FDA Inspection 611216 - 2009-07-30](https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/4d13a12d-f816-4a31-ad85-a222a64f6a6a)

Company: https://www.keypedia.com/companies/teksmart-fitness-llc/93cad6a7-e670-4bbb-aa58-25b4e05af59e

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