FDA Inspection 1018309 — Koko, LLC
The FDA completed an inspection of Koko, LLC on June 14, 2017 in Longmont, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 14, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Longmont, CO (United States)