FDA Inspection
Quintron Instrument Co IncQuintron Instrument Co Inc – FDA Inspection, Jun 16, 2017
Record Details
This FDA Inspection record concerns Quintron Instrument Co Inc, with an inspection on June 16, 2017, issued by the Minneapolis District Office, covering medical devices & rad health.
- Company
- Quintron Instrument Co Inc
- Inspection Date
- June 16, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 95e0fd14-cc14-441f-bc51-b05a93b33fe8
Inspection Facts
- Inspection number
- 1022603
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Quintron Instrument Co Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 2, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Quintron Instrument Co Inc
- FDA Inspection 984229 - 2016-03-02
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