FDA Inspection 569111 — Microtek Dominicana, S.A.
The FDA completed an inspection of Microtek Dominicana, S.A. on Jan 29, 2009 in La Romana. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 29, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- La Romana (Dominican Republic (the))