FDA Inspection 596433 — Avery Biomedical Devices, Inc.
The FDA completed an inspection of Avery Biomedical Devices, Inc. on July 10, 2009 in Commack, NY. 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 10, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Commack, NY (United States)