# FDA Inspection 1042236 - Trident Medical Products, Inc - February 23, 2018

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

> FDA Inspection 1042236 for Trident Medical Products, Inc on February 23, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042236
- Company Name: Trident Medical Products, Inc
- Inspection Date: 2018-02-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1042236 - 2018-02-23](https://www.globalkeysolutions.net/records/fda_inspections/trident-medical-products-inc/21142d63-4438-42a3-a9dd-73ba29967f9b)

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

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