FDA Inspection 684499 — EMD TECHNOLOGIES INCORPORATED

EMD TECHNOLOGIES INCORPORATED — FEI 3005894715

The FDA completed an inspection of EMD TECHNOLOGIES INCORPORATED on Sep 28, 2010 in Saint-Eustache. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 28, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Saint-Eustache (Canada)

Citations

IDCFRDescription
326421 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
544321 CFR 1020.30(g)Providing adequate assembly information

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.