# Celera Corporation – FDA Inspection, Jan 9, 2012

Source: https://www.keypedia.com/records/fda_inspections/celera-corporation/7088d8f3-731f-45c4-b021-2dd067af382a
Source feed: FDA_Inspections

> FDA inspection 761803 of Celera Corporation, January 09, 2012. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803, 806 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 761803
- Company Name: Celera Corporation
- Inspection Date: 2012-01-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 904397 - 2014-11-24](https://www.keypedia.com/records/fda_inspections/celera-corporation/6d051369-ac63-4776-9eab-ba9c00a0b544)
- FDA Inspection 646608 - 2009-11-05
- FDA Inspection 596438 - 2009-06-12

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