FDA Inspection 1010224 — STERIS Isomedix Puerto Rico, LLC.
The FDA completed an inspection of STERIS Isomedix Puerto Rico, LLC. on April 7, 2017 in Vega Alta, PR. 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
- April 7, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vega Alta, PR (United States)