FDA Inspection 1022776 — Needle Specialty Products Corporation
The FDA completed an inspection of Needle Specialty Products Corporation on June 1, 2017 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
- June 1, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Boyle, MS (United States)