FDA issued a Warning Letter to Myotronics-Noromed Inc. on 4/9/2012 for a later inspection.
483 Myotronics-Noromed Aug 2003

483 Myotronics-Noromed Aug 2003

Dennis Kawabata FDA, Catherine Laufmann FDA$595.00 - Available Now

FDA investigators audited the Myotronics-Noromed - Kent, WA, United States facility and issued inspectional observations (via FDA 483) on 15 Aug 2003.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Aug 2003
  • Location: Kent, United States
  • FEI: 3014732
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