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FDA Inspection 982331 — Compass Richmar LLC

Compass Richmar LLC — FEI 3004750362

The FDA completed an inspection of Compass Richmar LLC on July 14, 2016 in Chattanooga, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Chattanooga, TN (United States)

Facility

Other inspections at this facility

  • 889077 (VAI Wed Jul 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 789450 (OAI Thu Jun 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 741949 (OAI Wed Aug 24 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 575250 (VAI Thu Apr 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources