Teva API, Inc. – FDA Inspection, Jul 18, 2017

Record Details

This FDA Inspection record concerns Teva API, Inc., with an inspection on July 18, 2017, issued by the New Jersey District Office, covering medical devices & rad health.

Company: Teva API, Inc.
Inspection Date: July 18, 2017
Product Type: Medical Devices & Rad Health
Office: New Jersey District Office
Person: Peter R. Lenahan (FDA Associated Person)

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ID · aff4b425-2846-468c-89f0-cee1af1d3529

Inspection Facts

Inspection number: 1019140
FDA center: Medical Devices & Rad Health
Project area: Project Evaluation: Devices
Outcome: Form 483 issued

FDA Citations

21 CFR 812.40Sponsors' general responsibilities

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FDA Inspection

Teva API, Inc.July 18, 2017