FDA Inspection 764538 — Zimmer Biomet CMF and Thoracic LLC

Zimmer Biomet CMF and Thoracic LLC — FEI 1032347

The FDA completed an inspection of Zimmer Biomet CMF and Thoracic LLC on January 17, 2012 in Jacksonville, 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
January 17, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
337521 CFR 820.198(e)Records of complaint investigation