FDA Inspection
Seiler Instrument & Manufacturing Co. Inc.Seiler Instrument & Manufacturing Co. Inc. – FDA Inspection, Oct 19, 2017
Record Details
This FDA Inspection record concerns Seiler Instrument & Manufacturing Co. Inc., with an inspection on October 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c08568f6-34b9-4525-b5e9-61bf0279528c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1029315
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Seiler Instrument & Manufacturing Co. Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 17, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Seiler Instrument & Manufacturing Co. Inc.
- FDA Inspection 1221019 - 2023-10-17
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