FDA issued a Warning Letter to Dynavision International LLC on 9/5/2017 as a result of this inspection.
483 Dynavision International Apr 2017

483 Dynavision International Apr 2017

Christina Bigham FDA$119.00 - Available Now

FDA investigators audited the Dynavision International - West Chester, OH, United States facility and issued inspectional observations (via FDA 483) on 26 Apr 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 26 Apr 2017
  • Location: West Chester, United States
  • FEI: 3010197315
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