# Tingle X-Ray Products Inc – FDA Inspection, Jun 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/tingle-x-ray-products-inc/9de4dfcd-f74a-437f-ade0-7d6404d0fd09
Source feed: FDA_Inspections

> FDA inspection 1018344 of Tingle X-Ray Products Inc, June 23, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018344
- Company Name: Tingle X-Ray Products Inc
- Inspection Date: 2017-06-23
- 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 887526 - 2014-07-17
- [FDA Inspection 823246 - 2013-03-22](https://www.keypedia.com/records/fda_inspections/tingle-x-ray-products-inc/0f0d8f6b-59b1-4846-b4cf-77aa18a858b8)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/tingle-x-ray-products-inc/2fcf1608-4c8f-4377-9aff-bee9d90ee647

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