FDA Inspection
Multigon Industries IncMultigon Industries Inc – FDA Inspection, Sep 17, 2018
Record Details
This FDA Inspection record concerns Multigon Industries Inc, with an inspection on September 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 347f0d6c-2f5d-4bc3-a3d0-7813c12c98b9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1065931
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.72(b)Calibration procedures - content
- 21 CFR 820.72(a)Equipment control activity documentation
- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
- 21 CFR 820.70(a)Production processes
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Other FDA inspections of Multigon Industries Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 25, 2022 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 27, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 18, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 9, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Multigon Industries Inc
- FDA Inspection 1163355 - 2022-02-25
- FDA Inspection 921550 - 2015-03-27
- FDA Inspection 812052 - 2012-12-18
- FDA Inspection 704663 - 2010-12-09
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