# Preventive Technologies Inc – FDA Inspection, Apr 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/preventive-technologies-inc/7df53870-c007-46d1-8b45-3c126fc61a06
Source feed: FDA_Inspections

> FDA inspection 1049219 of Preventive Technologies Inc, April 19, 2018. Classification: Voluntary Action Indicated (VAI). 3 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: 1049219
- Company Name: Preventive Technologies Inc
- Inspection Date: 2018-04-19
- 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: 3

## Related Documents

- [FDA Inspection 905565 - 2014-11-21](https://www.keypedia.com/records/fda_inspections/preventive-technologies-inc/d556caa3-c584-4852-85ee-2e907f5da5a1)

## Related Officers

- [Investigator](https://www.keypedia.com/people/nydia-e-colon/c5137ded-6ae7-4855-b5b3-113bd851e1c3)

Company: https://www.keypedia.com/companies/preventive-technologies-inc/b4917d76-a37d-4b23-8174-a5b81b6293bf

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