FDA Inspection
SomnoMed Phillipines Inc.SomnoMed Phillipines Inc. – FDA Inspection, Jan 28, 2016
Record Details
This FDA Inspection record concerns SomnoMed Phillipines Inc., with an inspection on January 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- SomnoMed Phillipines Inc.
- Inspection Date
- January 28, 2016
- Product Type
- Devices
View Company Profile
ID · bf5a4d90-c577-4815-9591-db493058537c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 957017
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.86Acceptance status
- 21 CFR 820.40(a)Document review procedures, designated individual
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