FDA issued a Warning Letter to ProSun International, LLC on 10/25/2017 as a result of this inspection.
483 ProSun International Aug 2017

483 ProSun International Aug 2017

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FDA investigators audited the ProSun International - Saint Petersburg, FL, United States facility and issued inspectional observations (via FDA 483) on 04 Aug 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 04 Aug 2017
  • Location: Saint Petersburg, United States
  • FEI: 1000525872
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