# FDA Inspection 838131 - PT Products, LLC - June 27, 2013

Source: https://www.keypedia.com/records/fda_inspections/pt-products-llc/20919ac3-adc0-44f3-92c3-aa72fc8c4ac9
Source feed: FDA_Inspections

> FDA Inspection 838131 for PT Products, LLC on June 27, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838131
- Company Name: PT Products, LLC
- Inspection Date: 2013-06-27
- 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 838131 - 2013-06-27](https://www.keypedia.com/records/fda_inspections/pt-products-llc/7f37ab52-3337-4551-98d9-241ddec26300)
- [FDA Inspection 579699 - 2009-05-20](https://www.keypedia.com/records/fda_inspections/pt-products-llc/3d1c473e-aa10-47a7-8cef-3155495c0bc1)

Company: https://www.keypedia.com/companies/pt-products-llc/fac6cb22-c35e-4505-9dab-5e4088991661

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