FDA Inspection 965933 — Bellus Medical

Bellus Medical — FEI 3010392991

The FDA completed an inspection of Bellus Medical on March 23, 2016 in Johnson City, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 23, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Johnson City, TN (United States)