FDA Inspection 933247 — K2M, Inc.
The FDA completed an inspection of K2M, Inc. on July 6, 2015 in Leesburg, VA. 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
- July 6, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Leesburg, VA (United States)