FDA Inspection 741876 — Progressive Medical Inc

Progressive Medical Inc — FEI 3000236238

The FDA completed an inspection of Progressive Medical Inc on September 1, 2011 in Fenton, MO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Fenton, MO (United States)

Citations

IDCFRDescription
243021 CFR 820.30(b)Design plans - Lack of or inadequate
313021 CFR 820.100(a)Lack of or inadequate procedures
319921 CFR 820.40(a)Document review, approval documentation
342721 CFR 820.50(a)(2)Supplier oversight
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
44721 CFR 820.40Lack of procedures, or not maintained
63021 CFR 803.17Lack of Written MDR Procedures