# Allergan Pharmaceuticals Ireland – FDA Inspection, Jul 3, 2015

Source: https://www.keypedia.com/records/fda_inspections/allergan-pharmaceuticals-ireland/7d69a031-24c4-4f49-b2ff-c3775b5b0ae8
Source feed: FDA_Inspections

> FDA inspection 933338 of Allergan Pharmaceuticals Ireland, July 03, 2015. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 211 and 314. 8 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 933338
- Company Name: Allergan Pharmaceuticals Ireland
- Inspection Date: 2015-07-03
- 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: 5

## Related Documents

- [FDA Inspection 1259046 - 2025-01-30](https://www.keypedia.com/records/fda_inspections/allergan-pharmaceuticals-ireland/5cd0cdac-a1ee-429c-bf97-7a8c1777a54a)
- FDA Inspection 1194596 - 2022-06-17
- FDA Inspection 1117366 - 2018-05-04
- [FDA Inspection 1002463 - 2016-12-16](https://www.keypedia.com/records/fda_inspections/allergan-pharmaceuticals-ireland/f70e2599-43b0-412f-9cc1-6790f219ec6f)
- FDA Inspection 842267 - 2013-07-11

Company: https://www.keypedia.com/companies/allergan-pharmaceuticals-ireland/b65756b6-b7d5-438c-a312-93abdd3b372d

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