FDA issued a Warning Letter to Kelyniam Global, Inc. on 10/5/2017 as a result of this inspection.
483 Kelyniam Global May 2017

483 Kelyniam Global May 2017

$119 - Not in Stock

FDA investigators audited the Kelyniam Global - Collinsville, CT, United States facility and issued inspectional observations (via FDA 483) on 30 May 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 30 May 2017
  • Location: Collinsville, United States
  • FEI: 3009424796
Order