FDA Inspection 1097118 — Fehling Instruments GmbH & Co. KG
The FDA completed an inspection of Fehling Instruments GmbH & Co. KG on May 23, 2019 in Karlstein A. Main. 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
- May 23, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Karlstein A. Main (Germany)