FDA issued a Warning Letter to KVK-Tech, Inc on 2/11/2020 for a later inspection.
483 KVK-Tech Dec 2014

483 KVK-Tech Dec 2014

Gayle Lawson FDA, Tiffani Wilson FDA$119.00 - Available Now

FDA investigators audited the KVK-Tech - Newtown, PA, United States facility and issued inspectional observations (via FDA 483) on 11 Dec 2014.

Product details

  • Category: Human Drugs
  • Inspection end: 11 Dec 2014
  • Location: Newtown, United States
  • FEI: 3005117563
Add To Cart