FDA Inspection 1120455 — Kalitec Direct, LLC

Kalitec Direct, LLC — FEI 3009165919

The FDA completed an inspection of Kalitec Direct, LLC on March 4, 2020 in Sarasota, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 4, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sarasota, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures