FDA Inspection 833232 — Nexera Medical, Inc.

Nexera Medical, Inc. — FEI 3008010722

The FDA completed an inspection of Nexera Medical, Inc. on May 17, 2013 in Fort Lauderdale, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 17, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Lauderdale, FL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures