# Teksmart Fitness LLC – FDA Inspection, Jul 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/4d13a12d-f816-4a31-ad85-a222a64f6a6a
Source feed: FDA_Inspections

> FDA inspection 611216 of Teksmart Fitness LLC, July 30, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611216
- Company Name: Teksmart Fitness LLC
- Inspection Date: 2009-07-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1001756 - 2017-02-15
- [FDA Inspection 774747 - 2011-11-29](https://www.keypedia.com/records/fda_inspections/teksmart-fitness-llc/71763639-529d-4e89-8837-d5b226def1cb)

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