FDA Inspection
Fehling Instruments GmbH & Co. KGFehling Instruments GmbH & Co. KG – FDA Inspection, Mar 12, 2026
Record Details
This FDA Inspection record concerns Fehling Instruments GmbH & Co. KG, with an inspection on March 12, 2026, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- March 12, 2026
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · d608f7d3-a8a4-41d9-99f4-8ed91926214f
Inspection Facts
- Inspection number
- 1306904
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 803.50(a)(2)Individual Report of Malfunction
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Other FDA inspections of Fehling Instruments GmbH & Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 23, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 18, 2015 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Fehling Instruments GmbH & Co. KG
- FDA Inspection 1097118 - 2019-05-23
- FDA Inspection 933817 - 2015-06-18
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