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FDA Inspection
•Welch Allyn Inc•January 9, 2026

Welch Allyn Inc – FDA Inspection, Jan 9, 2026

Record Details

This FDA Inspection record concerns Welch Allyn Inc, with an inspection on January 9, 2026, issued by the New York District Office, covering medical devices & rad health.

Company
Welch Allyn Inc
Inspection Date
January 9, 2026
Product Type
Medical Devices & Rad Health
Office
New York District Office
People
  • Matthew D. Schnittker (Issuing Officer)
  • Wendy M. Stone (Company Rep)
View Company Profile

ID · ffdf253d-635d-4ff6-94dc-5de73f581146

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1298246
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

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

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Welch Allyn Inc

6
DateClassificationOfficeProject area
August 17, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
July 19, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
June 10, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
August 13, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
October 19, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
View all 6 other inspections on the company page
Other documents for Welch Allyn Inc
  • FDA Inspection 1215145 - 2023-08-17
  • FDA Inspection 1061645 - 2018-07-19
  • FDA Inspection 932308 - 2015-06-10
  • FDA Inspection 890794 - 2014-08-13
  • FDA Inspection 805650 - 2012-10-19

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