# CAMNTECH – FDA Inspection, Aug 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/camntech/5c847ef0-6baa-4384-80fd-c54c3a9a7a8b
Source feed: FDA_Inspections

> FDA inspection 1020179 of CAMNTECH, August 03, 2017. 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: 1020179
- Company Name: CAMNTECH
- Inspection Date: 2017-08-03
- 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 1262494 - 2025-01-16

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/andrea-a-branche/9ffe9b53-7963-49a6-be4e-25e644f1759f)

Company: https://www.keypedia.com/companies/camntech/5a2bcf5a-6123-4b31-93f0-4ee95cfa86a2

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