FDA Inspection 611216 — Teksmart Fitness LLC

Teksmart Fitness LLC — FEI 3006348601

The FDA completed an inspection of Teksmart Fitness LLC on Jul 30, 2009 in Minneapolis, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 30, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
317221 CFR 820.198(c)Investigation of device failures