FDA Inspection
Capsule Tech, IncCapsule Tech, Inc – FDA Inspection, Jun 16, 2011
Record Details
This FDA Inspection record concerns Capsule Tech, Inc, with an inspection on June 16, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Capsule Tech, Inc
- Inspection Date
- June 16, 2011
- Product Type
- Devices
View Company Profile
ID · 5a043e14-22c2-4eb3-a95a-0462f459ca2a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 730415
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.22Quality Audits - defined intervals
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of Capsule Tech, Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 26, 2018 | Not classified | New England District Office | |
| October 20, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 20, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 18, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Capsule Tech, Inc
- FDA Inspection 1109050 - 2018-10-26
- FDA Inspection 989624 - 2016-10-20
- FDA Inspection 989623 - 2016-10-20
- FDA Inspection 866410 - 2014-02-18
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