FDA Inspection
FUJIFILM Healthcare Manufacturing Corporation Sano OfficeFUJIFILM Healthcare Manufacturing Corporation Sano Office – FDA Inspection, Sep 10, 2019
Record Details
This FDA Inspection record concerns FUJIFILM Healthcare Manufacturing Corporation Sano Office, with an inspection on September 10, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 10, 2019
- Product Type
- Devices
View Company Profile
ID · 0f1da8a6-8b19-4bb6-a131-2a5d5394f215
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1114409
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of FUJIFILM Healthcare Manufacturing Corporation Sano Office
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 27, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 22, 2015 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for FUJIFILM Healthcare Manufacturing Corporation Sano Office
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.