FDA Inspection 966754 — Kegelmaster, Inc.
The FDA completed an inspection of Kegelmaster, Inc. on Feb 9, 2016 in Ocklawaha, FL. 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
- Feb 9, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Ocklawaha, FL (United States)