# Tech Group Europe Limited – FDA Inspection, Apr 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/tech-group-europe-limited/ece812d9-a930-4ef0-a8b4-05c0444a41de
Source feed: FDA_Inspections

> FDA inspection 1203759 of Tech Group Europe Limited, April 27, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203759
- Company Name: Tech Group Europe Limited
- Inspection Date: 2023-04-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1112546 - 2019-10-23

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sara-m-onyango/643c6ad3-9747-4bc2-9e8e-72f97b11e659)

Company: https://www.keypedia.com/companies/tech-group-europe-limited/fdd1a66b-0aed-4328-8d34-ef04491b34ec

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