# Hikma Pharmaceuticals USA INC. – FDA Inspection, Oct 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/hikma-pharmaceuticals-usa-inc/58697428-2935-48d0-b35b-b970969af19d
Source feed: FDA_Inspections

> FDA inspection 994023 of Hikma Pharmaceuticals USA INC., October 21, 2016. Classification: Official Action Indicated (OAI). 6 citations under 21 CFR parts 211 and 820. Form 483 issued. 27 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994023
- Company Name: Hikma Pharmaceuticals USA INC.
- Inspection Date: 2016-10-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Generic Drug Evaluation
- Product Type: Devices
- Center: Human Drugs
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)
- Issuing Officer
- Issuing Officer
- [FDA Associated Person](https://www.keypedia.com/people/matthew-b-casale/e78481c6-5fbd-4723-a79c-167176395af8)

Company: https://www.keypedia.com/companies/hikma-pharmaceuticals-usa-inc/6289cb89-1444-49a0-91b0-75a04e5152eb

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