FDA Inspection 1229959 — Lenkbar LLC
The FDA completed an inspection of Lenkbar LLC on Feb 6, 2024 in Naples, 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 6, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Naples, FL (United States)