FDA Inspection 1107078 — Proact Ltd

Proact Ltd — FEI 2183839

The FDA completed an inspection of Proact Ltd on Sep 12, 2019 in Centre Hall, PA. 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 12, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Centre Hall, PA (United States)

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