# FDA Inspection 865086 - Allergan - February 06, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/allergan/7f103d1b-75b1-4532-a4ce-46716c364fa3
Source feed: FDA_Inspections

> FDA Inspection 865086 for Allergan on February 06, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 865086
- Company Name: Allergan
- Inspection Date: 2014-02-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 865086 - 2014-02-06](https://www.globalkeysolutions.net/records/fda_inspections/allergan/1738be99-6194-4747-8efc-9aaea24e34a2)
- [FDA Inspection 800575 - 2012-08-22](https://www.globalkeysolutions.net/records/fda_inspections/allergan/73fa9295-e120-4378-b2ee-086ebe6fea96)
- [FDA Inspection 740227 - 2011-08-12](https://www.globalkeysolutions.net/records/fda_inspections/allergan/7c334243-e25b-427f-b9a5-213f8fb0e935)
- [FDA Inspection 740227 - 2011-08-12](https://www.globalkeysolutions.net/records/fda_inspections/allergan/b141da6c-077e-4590-8e8e-0e0b5f3d4118)

Company: https://www.globalkeysolutions.net/companies/allergan/6cd5e77a-d918-4099-a18c-4d424fd5bc1f

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