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FDA Inspection
•Nittobo Medical Company, Ltd., Medical Development Center•November 17, 2016

Nittobo Medical Company, Ltd., Medical Development Center – FDA Inspection, Nov 17, 2016

Record Details

This FDA Inspection record concerns Nittobo Medical Company, Ltd., Medical Development Center, with an inspection on November 17, 2016, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Nittobo Medical Company, Ltd., Medical Development Center
Inspection Date
November 17, 2016
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Cheryl D. Mccall (Issuing Officer)
View Company Profile

ID · 4e871abd-73a0-4bd4-8a30-1a7bfcd98fed

Inspection Facts

Inspection number
994522
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 803.17Lack of Written MDR Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Nittobo Medical Company, Ltd., Medical Development Center

2
DateClassificationOfficeProject area
July 9, 2026Not classifiedOffice of Inspections and Investigations
April 6, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Nittobo Medical Company, Ltd., Medical Development Center
  • FDA Inspection 1331290 - 2026-07-09
  • FDA Inspection 1206852 - 2023-04-06

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