FDA issued a Warning Letter to Diasol Inc on 9/28/2017 as a result of this inspection.
483 Diasol Jun 2017

483 Diasol Jun 2017

David Smith FDA$119.00 - Available Now

FDA investigators audited the Diasol - Phillipsburg, NJ, United States facility and issued inspectional observations (via FDA 483) on 15 Jun 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 15 Jun 2017
  • Location: Phillipsburg, United States
  • FEI: 3009491770
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