FDA issued a Warning Letter to TELEMED on 11/14/2017 as a result of this inspection.
483 TELEMED Aug 2017

483 TELEMED Aug 2017

Ashley Mutawakkil FDA$119.00 - Available Now

FDA investigators audited the TELEMED - Vilnius, Lithuania facility and issued inspectional observations (via FDA 483) on 03 Aug 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 03 Aug 2017
  • Location: Vilnius, Lithuania
  • FEI: 3007994837
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