FDA Inspection
Medi-Tech InternationalMedi-Tech International – FDA Inspection, Jun 4, 2015
Record Details
This FDA Inspection record concerns Medi-Tech International, with an inspection on June 4, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medi-Tech International
- Inspection Date
- June 4, 2015
- Product Type
- Devices
View Company Profile
ID · 2191576e-f362-4eca-adf1-d72a0898b501
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 929127
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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