FDA issued a Warning Letter to NAImco Inc dba Richmar Inc on 12/30/2011 for a previous inspection.
483 NAImco dba Richmar Jul 2014

483 NAImco dba Richmar Jul 2014

Wendy Blame FDA$119.00 - Available Now

FDA investigators audited the NAImco dba Richmar - Chattanooga, TN, United States facility and issued 7 inspectional observations (via FDA 483) on 30 Jul 2014.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 7
  • Inspection end: 30 Jul 2014
  • Location: Chattanooga, United States
  • FEI: 3004750362
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