FDA Inspection 1267031 — Beekley Corporation

Beekley Corporation — FEI 3000204334

The FDA completed an inspection of Beekley Corporation on Apr 9, 2025 in Bristol, CT. 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
Apr 9, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bristol, CT (United States)

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