FDA issued a Warning Letter to Diasol Inc. on 9/27/2017 for a previous inspection.
483 Diasol Sep 2018

483 Diasol Sep 2018

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FDA investigators audited the Diasol - San Fernando, CA, United States facility and issued inspectional observations (via FDA 483) on 28 Sep 2018.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 28 Sep 2018
  • Location: San Fernando, United States
  • FEI: 3002558569
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