FDA Inspection 569111 — Microtek Dominicana, S.A.
The FDA completed an inspection of Microtek Dominicana, S.A. on January 29, 2009 in La Romana. 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
- January 29, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- La Romana (Dominican Republic (the))