# Trident Medical Products, Inc – FDA Inspection, Feb 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/trident-medical-products-inc/ace87918-5f2b-48e8-a790-f590ce7ad04a
Source feed: FDA_Inspections

> FDA inspection 1042236 of Trident Medical Products, Inc, February 23, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1042236
- Company Name: Trident Medical Products, Inc
- Inspection Date: 2018-02-23
- 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: 2

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jeremy-l-stukes/03812740-3c4d-4b11-9da3-44b7a03d72b1)

Company: https://www.keypedia.com/companies/trident-medical-products-inc/06d88c57-8d60-4747-9c09-1b7c508b4459

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