FDA Inspection 1005518 — Molded Products Inc

Molded Products Inc — FEI 1000138417

The FDA completed an inspection of Molded Products Inc on Mar 10, 2017 in Harlan, IA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Harlan, IA (United States)

Citations

IDCFRDescription
419221 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))