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FDA Inspection
•TELEMED•February 12, 2026

TELEMED – FDA Inspection, Feb 12, 2026

Record Details

This FDA Inspection record concerns TELEMED, with an inspection on February 12, 2026, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
TELEMED
Inspection Date
February 12, 2026
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Benjamin E. Bowen (Investigator)
View Company Profile

ID · fae1befd-a870-4609-a560-458980cf4b86

Inspection Facts

Inspection number
1302590
FDA center
Medical Devices & Rad Health
Project area
Compliance: Medical Devices
Outcome
Form 483 issued

FDA Citations

1
  1. ISO 13485:2016 Clause 8.5.2Corrective action procedures not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of TELEMED

3
DateClassificationOfficeProject area
March 16, 2023VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
December 13, 2018Not classifiedOffice of Inspections and InvestigationsCompliance: Devices
August 3, 2017Not classifiedOffice of Inspections and Investigations
Other documents for TELEMED
  • FDA Inspection 1199983 - 2023-03-16
  • FDA Inspection 1075788 - 2018-12-13
  • FDA Inspection 1021806 - 2017-08-03

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