# FDA Inspection 1214529 - Titan Manufacturing, Inc. - August 09, 2023

Source: https://www.keypedia.com/records/fda_inspections/titan-manufacturing-inc/ba67f1ff-d9ad-4033-b27e-2c37837669d1
Source feed: FDA_Inspections

> FDA Inspection 1214529 for Titan Manufacturing, Inc. on August 09, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1214529
- Company Name: Titan Manufacturing, Inc.
- Inspection Date: 2023-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1214529 - 2023-08-09](https://www.keypedia.com/records/fda_inspections/titan-manufacturing-inc/1a8b8447-c6ef-4f79-875c-86defe9a0e46)
- [FDA Inspection 1049440 - 2018-03-26](https://www.keypedia.com/records/fda_inspections/titan-manufacturing-inc/3ab4d008-79b6-4062-ba86-f9ee52de8adf)

Company: https://www.keypedia.com/companies/titan-manufacturing-inc/28ceb353-c856-4d31-910f-f9d7f87e4b4b

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