FDA Inspection 988501 — HERSILL, S.L.

HERSILL, S.L. — FEI 3007360714

The FDA completed an inspection of HERSILL, S.L. on Sep 20, 2016 in Mostoles. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 20, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Mostoles (Spain)

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