FDA issued a Warning Letter to CoRE Labs, LLC on 2/20/2013 for a previous inspection.
483 CoRE labs Dec 2016

483 CoRE labs Dec 2016

Kathleen Tormey FDA$119.00 - Available Now

FDA investigators audited the CoRE labs - Englewood, CO, United States facility and issued 2 inspectional observations (via FDA 483) on 12 Dec 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 2
  • Inspection end: 12 Dec 2016
  • Location: Englewood, United States
  • FEI: 3001620005
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