FDA Inspection 1094896 — Heitec Ag

Heitec Ag — FEI 3011436471

The FDA completed an inspection of Heitec Ag on May 27, 2019 in Eckental. 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
May 27, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Eckental (Germany)