# RAPID RELEASE TECHNOLOGIES – FDA Inspection, Aug 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/rapid-release-technologies/ad65db70-3601-4683-9837-13ef827a9f9d
Source feed: FDA_Inspections

> FDA inspection 1024368 of RAPID RELEASE TECHNOLOGIES, August 24, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024368
- Company Name: RAPID RELEASE TECHNOLOGIES
- Inspection Date: 2017-08-24
- 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: 0

## Related Documents

- [FDA Inspection 977555 - 2016-05-25](https://www.keypedia.com/records/fda_inspections/rapid-release-technologies/fe323638-cfe5-48a5-a629-3fbf3191c1a3)
- FDA Inspection 933507 - 2015-07-06

## Related Officers

- [Company Rep](https://www.keypedia.com/people/juanita-banuelos/b8b581ef-b9f3-4d77-a9fa-691223dbb7f4)

Company: https://www.keypedia.com/companies/rapid-release-technologies/f499076b-7864-4a37-b987-6ea6594c79e9

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