# FDA Inspection 592318 - Neutron Products - June 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/neutron-products/732ede62-c7d0-4b0b-beaf-ff241684bccc
Source feed: FDA_Inspections

> FDA Inspection 592318 for Neutron Products on June 11, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 592318
- Company Name: Neutron Products
- Inspection Date: 2009-06-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 827934 - 2013-04-17](https://www.keypedia.com/records/fda_inspections/neutron-products/56ceb6de-a697-45b1-8533-01638df1c909)

Company: https://www.keypedia.com/companies/neutron-products/95b2f15d-391c-4695-a926-9d1802f94f21

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