FDA Inspection 902069 — MDPO, LLC

MDPO, LLC — FEI 3008525119

The FDA completed an inspection of MDPO, LLC on Oct 27, 2014 in Southwest Ranches, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 8 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 27, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Southwest Ranches, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1471821 CFR 820.30(g)Design validation - Risk analysis
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
237121 CFR 820.30(a)Design control - no procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
44721 CFR 820.40Lack of procedures, or not maintained
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures