# Trinity Sterile,  Inc. – FDA Inspection, Mar 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/0ccbdadd-6214-4d70-8a6b-e6f0c98a1d28
Source feed: FDA_Inspections

> FDA inspection 1004661 of Trinity Sterile,  Inc., March 13, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004661
- Company Name: Trinity Sterile,  Inc.
- Inspection Date: 2017-03-13
- 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: 9

## Related Documents

- [FDA Inspection 1239929 - 2024-05-23](https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/71461b33-4e79-436e-9f99-89f286ecd90b)
- [FDA Inspection 1087531 - 2019-04-26](https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/87443545-1294-488a-bec4-b7e3b9f73135)
- FDA Inspection 818470 - 2013-02-13
- FDA Inspection 678565 - 2010-09-01

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

Company: https://www.keypedia.com/companies/trinity-sterile-inc/3f7ce0d7-636b-463b-ad3f-bdbac7edeb4c

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