# Tetracore, Inc. – FDA Inspection, May 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/tetracore-inc/d5d7daf2-2014-43fb-8d03-1588fb17664f
Source feed: FDA_Inspections

> FDA inspection 584280 of Tetracore, Inc., May 28, 2009. Classification: Official Action Indicated (OAI). 4 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 584280
- Company Name: Tetracore, Inc.
- Inspection Date: 2009-05-28
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1256176 - 2024-12-05
- FDA Inspection 1167551 - 2022-04-08
- FDA Inspection 1111969 - 2019-12-06
- [FDA Inspection 842712 - 2013-08-14](https://www.keypedia.com/records/fda_inspections/tetracore-inc/4ecb8899-ef84-44f7-b56b-740fec06a4e5)
- FDA Inspection 669356 - 2010-06-28

Company: https://www.keypedia.com/companies/tetracore-inc/f7bc78b5-c7b9-4c9c-9220-893497f82627

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