FDA Inspection 1008979 — Kalitec Direct, LLC

Kalitec Direct, LLC — FEI 3009165919

The FDA completed an inspection of Kalitec Direct, LLC on April 13, 2017 in Sarasota, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sarasota, FL (United States)

Citations

IDCFRDescription
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures