FDA Inspection 563008 — Alliqua Biomedical
The FDA completed an inspection of Alliqua Biomedical on February 18, 2009 in Langhorne, PA. 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 18, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Langhorne, PA (United States)