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