483 Coloplast Manufacturing US Sep 2011

483 Coloplast Manufacturing US Sep 2011

Jessica Johnson FDA$119.00 - Available Now

FDA investigators audited the Coloplast Manufacturing US - Minneapolis, MN, United States facility and issued 1 inspectional observation (via FDA 483) on 28 Sep 2011.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 1
  • Inspection end: 28 Sep 2011
  • Location: Minneapolis, United States
  • FEI: 2125050
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