FDA Inspection
OMNIA SRLOMNIA SRL – FDA Inspection, Dec 15, 2016
Record Details
This FDA Inspection record concerns OMNIA SRL, with an inspection on December 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · aa22d294-2ca7-4e4f-8315-51908cabb420
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1000062
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.70(a)Production processes
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