FDA Inspection 848920 — Moog Costa Rica, SRL

Moog Costa Rica, SRL — FEI 3008058400

The FDA completed an inspection of Moog Costa Rica, SRL on Sep 19, 2013 in Alajuela. 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
Sep 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Alajuela (Costa Rica)

Citations

IDCFRDescription
44721 CFR 820.40Lack of procedures, or not maintained

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