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FDA Inspection
•Capsule Tech, Inc•October 26, 2018

Capsule Tech, Inc – FDA Inspection, Oct 26, 2018

Record Details

This FDA Inspection record concerns Capsule Tech, Inc, with an inspection on October 26, 2018, issued by the New England District Office, covering medical devices & rad health.

Company
Capsule Tech, Inc
Inspection Date
October 26, 2018
Product Type
Medical Devices & Rad Health
Office
New England District Office
View Company Profile

ID · 6984b3b1-0bb0-4a23-9870-fd78552d1476

Inspection Facts

Inspection number
1109050
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Capsule Tech, Inc

4
DateClassificationOfficeProject area
October 20, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
October 20, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
February 18, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 16, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Capsule Tech, Inc
  • FDA Inspection 989624 - 2016-10-20
  • FDA Inspection 989623 - 2016-10-20
  • FDA Inspection 866410 - 2014-02-18
  • FDA Inspection 730415 - 2011-06-16

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