FDA Inspection
Transoma MedicalTransoma Medical – FDA Inspection, Aug 28, 2009
Record Details
This FDA Inspection record concerns Transoma Medical, with an inspection on August 28, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Transoma Medical
- Inspection Date
- August 28, 2009
- Product Type
- Devices
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ID · fe4ebbd3-3669-437f-8fc3-c63b7755d241
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 606323
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)(3)Processing MDRs {see also 803, 804}
- 21 CFR 820.198(a)(1)Uniform and timely processing
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