# FDA Inspection 1073650 - Ti-Ba Enterprises, Inc. - December 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ti-ba-enterprises-inc/dd28b566-3781-444d-b81e-a20f97e22874
Source feed: FDA_Inspections

> FDA Inspection 1073650 for Ti-Ba Enterprises, Inc. on December 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073650
- Company Name: Ti-Ba Enterprises, Inc.
- Inspection Date: 2018-12-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1197496 - 2023-02-10](https://www.globalkeysolutions.net/records/fda_inspections/ti-ba-enterprises-inc/8d3cc36a-7e31-4e10-a421-64212568ab36)
- [FDA Inspection 1073650 - 2018-12-03](https://www.globalkeysolutions.net/records/fda_inspections/ti-ba-enterprises-inc/7018d1d4-1478-4e70-82d4-cfc21f1e2997)

Company: https://www.globalkeysolutions.net/companies/ti-ba-enterprises-inc/5f96f1cf-2c07-4688-b49a-966e134547e9

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