# FDA Inspection 842712 - Tetracore, Inc. - August 14, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/4ecb8899-ef84-44f7-b56b-740fec06a4e5
Source feed: FDA_Inspections

> FDA Inspection 842712 for Tetracore, Inc. on August 14, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 842712
- Company Name: Tetracore, Inc.
- Inspection Date: 2013-08-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1256176 - 2024-12-05](https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/02c1e280-6443-4cdf-9bf7-246f96cafe12)
- [FDA Inspection 1256176 - 2024-12-05](https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/5d39328f-ee21-48cd-853e-90d29c831191)
- [FDA Inspection 1256176 - 2024-12-05](https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/6c3b4be5-d5ef-426b-8803-e5814ca093ba)
- [FDA Inspection 1167551 - 2022-04-08](https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/3decc77b-a054-4050-8e95-ebeb93e697d4)
- [FDA Inspection 1167551 - 2022-04-08](https://www.globalkeysolutions.net/records/fda_inspections/tetracore-inc/16f7572e-9106-41e2-858e-3510a4b8f577)

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

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