# Tingle X-Ray Products Inc, Cottondale, AL – FDA Inspections

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

> Inspection records and compliance data for Tingle X-Ray Products Inc in Cottondale, Alabama. 3 FDA inspections on record (1 OAI), last inspected June 23, 2017.

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## Details

- Name: Tingle X-Ray Products Inc
- FEI Number: 3002539637
- Address Line 1: 5481 Skyland Blvd E
- City: Cottondale
- State: Alabama
- Zip Code: 35453
- Country Name: United States
- Address: 5481 Skyland Blvd E, Cottondale, Alabama 35453, United States
- Country: United States

## Related Documents

- FDA Inspection 1018344 - Tingle X-Ray Products Inc - 2017-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2017
- [FDA Inspection 1018344 - Tingle X-Ray Products Inc - 2017-06-23](https://www.keypedia.com/records/fda_inspections/tingle-x-ray-products-inc/9de4dfcd-f74a-437f-ade0-7d6404d0fd09) — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2017
- FDA Inspection 1018344 - Tingle X-Ray Products Inc - 2017-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2017
- FDA Inspection 887526 - Tingle X-Ray Products Inc - 2014-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2014
- FDA Inspection 887526 - Tingle X-Ray Products Inc - 2014-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2014
- FDA Inspection 887526 - Tingle X-Ray Products Inc - 2014-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2014
- [FDA Inspection 823246 - Tingle X-Ray Products Inc - 2013-03-22](https://www.keypedia.com/records/fda_inspections/tingle-x-ray-products-inc/0f0d8f6b-59b1-4846-b4cf-77aa18a858b8) — classification: Official Action Indicated (OAI), source: FDA, date: March 22, 2013
- FDA Inspection 823246 - Tingle X-Ray Products Inc - 2013-03-22 — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2013
- FDA Inspection 823246 - Tingle X-Ray Products Inc - 2013-03-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 22, 2013

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