FDA issued a Warning Letter to Nordimex, LLC on 10/11/2011 as a result of this inspection.
483 OPMX May 2011

483 OPMX May 2011

Zachary Bogorad FDA, Sara Dent Acosta FDA$119.00 - Available Now

FDA investigators audited the OPMX - San Diego, CA, United States facility and issued 3 inspectional observations (via FDA 483) on 31 May 2011.

Product details

  • Category: Foods & Cosmetics / Human Drugs
  • Number of Observations: 3
  • Inspection end: 31 May 2011
  • Location: San Diego, United States
  • FEI: 3008937007
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