# FDA Inspection 1239929 - Trinity Sterile,  Inc. - May 23, 2024

Source: https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/71461b33-4e79-436e-9f99-89f286ecd90b
Source feed: FDA_Inspections

> FDA Inspection 1239929 for Trinity Sterile,  Inc. on May 23, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1239929
- Company Name: Trinity Sterile,  Inc.
- Inspection Date: 2024-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 1004661 - 2017-03-13](https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/0ccbdadd-6214-4d70-8a6b-e6f0c98a1d28)
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- [FDA Inspection 818470 - 2013-02-13](https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/3019b61e-dec0-4152-b27f-2a39c7925c22)
- [FDA Inspection 678565 - 2010-09-01](https://www.keypedia.com/records/fda_inspections/trinity-sterile-inc/e1a3d078-6c13-4d9a-b0fd-f0c7cedc8ee0)

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