FDA Inspection
Flexbar Machine CorpFlexbar Machine Corp – FDA Inspection, Oct 30, 2009
Record Details
This FDA Inspection record concerns Flexbar Machine Corp, with an inspection on October 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Flexbar Machine Corp
- Inspection Date
- October 30, 2009
- Product Type
- Devices
View Company Profile
ID · a287a1cc-38a5-4aa2-a538-55cd8146e835
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 625749
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(a)(1)Uniform and timely processing
- 21 CFR 803.17(b)(2)Reports and information documentation
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Other FDA inspections of Flexbar Machine Corp
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 4, 2025 | NAI | New York District Office | Compliance: Medical Devices |
| April 4, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 22, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 1, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Flexbar Machine Corp
- FDA Inspection 1266364 - 2025-04-04
- FDA Inspection 1047534 - 2018-04-04
- FDA Inspection 888627 - 2014-07-22
- FDA Inspection 779265 - 2012-05-01
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