# FDA Inspection 816931 - Cambridge Diagnostic Products, Inc. - January 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/cambridge-diagnostic-products-inc/beb8d342-c868-4214-8785-c16534bb93e7
Source feed: FDA_Inspections

> FDA Inspection 816931 for Cambridge Diagnostic Products, Inc. on January 10, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 816931
- Company Name: Cambridge Diagnostic Products, Inc.
- Inspection Date: 2013-01-10
- 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 1201734 - 2023-03-16](https://www.keypedia.com/records/fda_inspections/cambridge-diagnostic-products-inc/f4bb3735-2c17-4c5c-8cc4-7eca1ba200a2)
- [FDA Inspection 1201734 - 2023-03-16](https://www.keypedia.com/records/fda_inspections/cambridge-diagnostic-products-inc/ade4b886-17f2-417d-9ace-399cb172ab38)
- [FDA Inspection 816931 - 2013-01-10](https://www.keypedia.com/records/fda_inspections/cambridge-diagnostic-products-inc/fc4e7e67-eefd-4d9b-b471-146f5d30784a)

Company: https://www.keypedia.com/companies/cambridge-diagnostic-products-inc/ee9b8d32-0ef6-4915-91e4-915ee72bf41e

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