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Kenji Ando, M.D., Kitakyushu, Japan – FDA Inspections

Inspection records and compliance data for Kenji Ando, M.D. in Kitakyushu. 2 FDA inspections on record, last inspected October 31, 2019.

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Company Profile

This profile covers Kenji Ando, M.D. based in Kitakyushu, Japan.

FDA Inspection History

FDA inspections
2
OAI
0
VAI
2
NAI
0
Form 483s
0
Warning letters
0

First inspected July 17, 2014. Last inspected October 31, 2019.

Most cited issue areas

  • Investigator non-compliance with agreement/plan/regulations1 inspection

FDA inspections (2)

DateResultFDA center(s)Insp. #
October 31, 2019VAIMedical Devices & Rad Health · Bioresearch Monitoring1110723
July 17, 2014VAIMedical Devices & Rad Health · Bioresearch Monitoring893786
FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

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J. Morita Mfg. Corp.
NIDEK Co., Ltd.
Stryker Medtech K.K.
Denka Seiken Co., Ltd. - Niigata Factory
Okamoto Industries Inc.
ARS, Inc.
Company Information

Name

Kenji Ando, M.D.

FEI Number

1000585154

Address

Asano; Kokurakita Asano; Kokurakita; Kokurakita; 3chome 2-1; Yoshino-Machi; Kokurakita, Kitakyushu, Japan

Country

Japan

ID: e8c58c78-4ae5-42ae-be2b-bfd3b9562f3f

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