FDA Inspection
Teksmart Fitness LLCTeksmart Fitness LLC – FDA Inspection, Jul 30, 2009
Record Details
This FDA Inspection record concerns Teksmart Fitness LLC, with an inspection on July 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Teksmart Fitness LLC
- Inspection Date
- July 30, 2009
- Product Type
- Devices
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ID · 4d13a12d-f816-4a31-ad85-a222a64f6a6a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 611216
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Teksmart Fitness LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 15, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 29, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Teksmart Fitness LLC
- FDA Inspection 1001756 - 2017-02-15
- FDA Inspection 774747 - 2011-11-29
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