# TIDI Products, LLC – FDA Inspection, May 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/tidi-products-llc/a89b5710-367a-47be-a726-535eb8b60621
Source feed: FDA_Inspections

> FDA inspection 1055339 of TIDI Products, LLC, May 30, 2018. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055339
- Company Name: TIDI Products, LLC
- Inspection Date: 2018-05-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1161536 - 2021-12-09
- FDA Inspection 885452 - 2014-06-25
- FDA Inspection 681404 - 2010-09-15
- FDA Inspection 656041 - 2010-04-06

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)

Company: https://www.keypedia.com/companies/tidi-products-llc/b2a33c6c-ae29-4f6e-a338-f7407337394c

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