# TELEMED – FDA Inspection, Mar 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/telemed/d4f3c781-e37f-4278-a2ee-63f20e500d5d
Source feed: FDA_Inspections

> FDA inspection 1199983 of TELEMED, March 16, 2023. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199983
- Company Name: TELEMED
- Inspection Date: 2023-03-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1302590 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/telemed/fae1befd-a870-4609-a560-458980cf4b86)
- [FDA Inspection 1075788 - 2018-12-13](https://www.keypedia.com/records/fda_inspections/telemed/e8b32b2a-98a0-4597-801a-6bed0596e92b)
- [FDA Inspection 1021806 - 2017-08-03](https://www.keypedia.com/records/fda_inspections/telemed/b9e70a17-2f61-4a68-8616-a78b6d583484)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/telemed/fb7c3006-78df-400d-ae72-7327e54a0145

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7