FDA Inspection
Thornhill Research IncThornhill Research Inc – FDA Inspection, Nov 19, 2015
Record Details
This FDA Inspection record concerns Thornhill Research Inc, with an inspection on November 19, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Thornhill Research Inc
- Inspection Date
- November 19, 2015
- Product Type
- Devices
View Company Profile
ID · 923be79d-30cd-4468-84a4-e9202346740e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 952340
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 806.10(a)(1)Report of risk to health
- 21 CFR 820.72(a)Equipment suitability & capability
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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