# FDA Inspection 676236 - The Ritedose Corporation - August 12, 2010

Source: https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/09fd35d7-c3cc-4e71-bd1e-a346bacb00f7
Source feed: FDA_Inspections

> FDA Inspection 676236 for The Ritedose Corporation on August 12, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 676236
- Company Name: The Ritedose Corporation
- Inspection Date: 2010-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250871 - 2025-02-28](https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/a638648e-fc4d-4d6f-a757-610ee0f71120)
- [FDA Inspection 1165123 - 2022-03-22](https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/601e17c0-c4fc-47e4-950e-7a4183dcae93)
- [FDA Inspection 1089541 - 2019-04-18](https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/2eb6871a-e581-45f6-a645-8912fc5af088)
- [FDA Inspection 1015894 - 2017-03-03](https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/67b96a15-dd74-4d6a-860c-491633de72c6)
- [FDA Inspection 1015894 - 2017-03-03](https://www.keypedia.com/records/fda_inspections/the-ritedose-corporation/a5ca351d-8c5a-491e-9500-e6796c673502)

Company: https://www.keypedia.com/companies/the-ritedose-corporation/eb3f4c46-57bb-4bd6-a3ee-0fa0517ce0fa

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