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FDA Inspection
•Elucid Bioimaging Inc.•March 20, 2026

Elucid Bioimaging Inc. – FDA Inspection, Mar 20, 2026

Record Details

This FDA Inspection record concerns Elucid Bioimaging Inc., with an inspection on March 20, 2026, issued by the New England District Office, covering medical devices & rad health.

Company
Elucid Bioimaging Inc.
Inspection Date
March 20, 2026
Product Type
Medical Devices & Rad Health
Office
New England District Office
Person
  • James P. Finn (Company Rep)
View Company Profile

ID · a0be587d-6b31-48a7-8101-de82c1cdef3e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1308272
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Elucid Bioimaging Inc.

1
DateClassificationOfficeProject area
April 2, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Elucid Bioimaging Inc.
  • FDA Inspection 1084923 - 2019-04-02

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