Precimade – FDA Inspection, Oct 26, 2016

Record Details

This FDA Inspection record concerns Precimade, with an inspection on October 26, 2016, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company: Precimade
Inspection Date: October 26, 2016
Product Type: Medical Devices & Rad Health
Office: Office of Inspections and Investigations
Person: Stephen D. Eich (Company Rep)

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ID · 0854878d-427b-46d0-9f94-83e8c930473f

Inspection Facts

Inspection number: 992411
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices
Outcome: Form 483 issued

FDA Citations

21 CFR 820.100(a)Lack of or inadequate procedures

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FDA Inspection

PrecimadeOctober 26, 2016