Omni Manufacturing Services S.A. de C.V. – FDA Inspection, Jun 28, 2018

Record Details

This FDA Inspection record concerns Omni Manufacturing Services S.A. de C.V., with an inspection on June 28, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Omni Manufacturing Services S.A. de C.V.
Inspection Date: June 28, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Suzanne M. Healy (FDA Associated Person)

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ID · e0e5950c-8e5f-45df-8a5b-9295aa8d3faf

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1057263
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices
Outcome: Form 483 issued

FDA Citations

21 CFR 820.75(c)Documentation - review in response to changes or deviations

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FDA Inspection

Omni Manufacturing Services S.A. de C.V.June 28, 2018