FDA Inspection 786093 — Omega Laboratories Inc

Omega Laboratories Inc — FEI 3004847291

The FDA completed an inspection of Omega Laboratories Inc on Apr 26, 2012 in Mogadore, OH. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Mogadore, OH (United States)

Citations

IDCFRDescription
237121 CFR 820.30(a)Design control - no procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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