FDA issued a Warning Letter to KVK-Tech, Inc on 2/11/2020 for a later inspection.
483 KVK-Tech Mar 2016

483 KVK-Tech Mar 2016

$119 - Not in Stock

FDA investigators audited the KVK-Tech - Newtown, PA, United States facility and issued inspectional observations (via FDA 483) on 14 Mar 2016.

Product details

  • Category: Human Drugs
  • Inspection end: 14 Mar 2016
  • Location: Newtown, United States
  • FEI: 3005117563
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