# Alza Corporation – FDA Inspection, Feb 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/alza-corporation/ea30a6c6-c924-4074-84da-b9ef6416bef2
Source feed: FDA_Inspections

> FDA inspection 1039728 of Alza Corporation, February 01, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 211. Form 483 issued. 8 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039728
- Company Name: Alza Corporation
- Inspection Date: 2018-02-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 982489 - 2016-06-29
- [FDA Inspection 897977 - 2014-09-19](https://www.keypedia.com/records/fda_inspections/alza-corporation/74c0dddc-c14b-4afd-9041-7e7519c1d267)
- FDA Inspection 870168 - 2014-03-14
- FDA Inspection 829365 - 2013-03-22
- [FDA Inspection 777640 - 2012-04-12](https://www.keypedia.com/records/fda_inspections/alza-corporation/0ba5aed2-0b8d-40d1-b0fa-0034cb1ba394)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/lucila-b-nwatu/3d1c9670-8206-425c-bddd-32e395293042)

Company: https://www.keypedia.com/companies/alza-corporation/88512ed8-3e3d-4510-b9d9-b7d743b87343

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