# FDA Inspection 904397 - Celera Corporation - November 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/celera-corporation/6d051369-ac63-4776-9eab-ba9c00a0b544
Source feed: FDA_Inspections

> FDA Inspection 904397 for Celera Corporation on November 24, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 904397
- Company Name: Celera Corporation
- Inspection Date: 2014-11-24
- 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 904397 - 2014-11-24](https://www.keypedia.com/records/fda_inspections/celera-corporation/3271a69e-41f5-433e-baa3-b97d2a1bd681)
- [FDA Inspection 904397 - 2014-11-24](https://www.keypedia.com/records/fda_inspections/celera-corporation/597c931f-ca54-41a4-ba34-a9f364baa84a)
- [FDA Inspection 761803 - 2012-01-09](https://www.keypedia.com/records/fda_inspections/celera-corporation/7088d8f3-731f-45c4-b021-2dd067af382a)
- [FDA Inspection 761803 - 2012-01-09](https://www.keypedia.com/records/fda_inspections/celera-corporation/49d5c48d-cc27-4e68-9ff2-3be2ff3c033c)
- [FDA Inspection 646608 - 2009-11-05](https://www.keypedia.com/records/fda_inspections/celera-corporation/ac7802a5-774b-4dc2-b2dc-74414ffd86aa)

Company: https://www.keypedia.com/companies/celera-corporation/03a7f1b1-793b-47a3-9a48-d7a5107661e3

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