FDA Inspection 648881 — AMD Medicom Inc.
The FDA completed an inspection of AMD Medicom Inc. on February 1, 2010 in Tonawanda, 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
- February 1, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Tonawanda, NY (United States)