FDA Inspection 595573 — Needle Specialty Products Corporation
The FDA completed an inspection of Needle Specialty Products Corporation on July 7, 2009 in Boyle, MS. 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 7, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boyle, MS (United States)