FDA Inspection
Diversatek HealthcareDiversatek Healthcare – FDA Inspection, Jun 25, 2012
Record Details
This FDA Inspection record concerns Diversatek Healthcare, with an inspection on June 25, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Diversatek Healthcare
- Inspection Date
- June 25, 2012
- Product Type
- Devices
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ID · d2a253f4-70ec-46fb-b0b8-a28ce6be9b0f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 791104
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(c)Investigation of device failures
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Other FDA inspections of Diversatek Healthcare
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 5, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 29, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 20, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Diversatek Healthcare
- FDA Inspection 1178591 - 2022-08-05
- FDA Inspection 977968 - 2016-06-29
- FDA Inspection 584731 - 2009-03-20
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