FDA Inspection
Geminga MedicalGeminga Medical – FDA Inspection, Feb 24, 2015
Record Details
This FDA Inspection record concerns Geminga Medical, with an inspection on February 24, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Geminga Medical
- Inspection Date
- February 24, 2015
- Product Type
- Devices
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ID · 5b8d0615-6ede-4d8f-9ab1-f0ee895220cb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 916566
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.75(a)Lack of or inadequate process validation
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