# Angelini Pharma, Inc. – FDA Inspection, Sep 2, 2016

Source: https://www.keypedia.com/records/fda_inspections/angelini-pharma-inc/88448e94-8938-427f-8816-35d8c4693202
Source feed: FDA_Inspections

> FDA inspection 989300 of Angelini Pharma, Inc., September 02, 2016. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 806 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989300
- Company Name: Angelini Pharma, Inc.
- Inspection Date: 2016-09-02
- 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: 7

## Related Documents

- [FDA Inspection 920215 - 2015-03-17](https://www.keypedia.com/records/fda_inspections/angelini-pharma-inc/b3940b75-c31b-4396-bbd6-323c79e33985)
- FDA Inspection 875272 - 2014-04-22
- FDA Inspection 740481 - 2011-08-19

Company: https://www.keypedia.com/companies/angelini-pharma-inc/2a6ee7df-9c30-4af7-a6ba-aabcdd66fde1

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