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FDA Inspection
•Euroimmun Medizinische Labordiagnostika Ag•November 4, 2016

Euroimmun Medizinische Labordiagnostika Ag – FDA Inspection, Nov 4, 2016

Record Details

This FDA Inspection record concerns Euroimmun Medizinische Labordiagnostika Ag, with an inspection on November 4, 2016, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Euroimmun Medizinische Labordiagnostika Ag
Inspection Date
November 4, 2016
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Li Li (Issuing Officer)
View Company Profile

ID · b4b43a40-b43b-4496-9587-4022c9b4f80c

Inspection Facts

Inspection number
1002335
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.100(a)Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

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