# FDA Inspection 864605 - TIDI Products, LLC - January 31, 2014

Source: https://www.keypedia.com/records/fda_inspections/tidi-products-llc/7c7ffcf7-35ee-435c-8402-04bcf5f7c19e
Source feed: FDA_Inspections

> FDA Inspection 864605 for TIDI Products, LLC on January 31, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 864605
- Company Name: TIDI Products, LLC
- Inspection Date: 2014-01-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 809068 - 2012-11-27](https://www.keypedia.com/records/fda_inspections/tidi-products-llc/30b02ff8-e495-4c81-bca4-bd8d80163855)
- [FDA Inspection 661945 - 2010-05-10](https://www.keypedia.com/records/fda_inspections/tidi-products-llc/2afef422-6970-49de-9a29-59d755e9192b)

Company: https://www.keypedia.com/companies/tidi-products-llc/5991aae5-80e1-4e48-8524-62a759a21909

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