FDA Inspection
Angiplast Private LimitedAngiplast Private Limited – FDA Inspection, Jun 15, 2017
Record Details
This FDA Inspection record concerns Angiplast Private Limited, with an inspection on June 15, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Angiplast Private Limited
- Inspection Date
- June 15, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · bd87b873-2404-4ae5-ad86-e764c9f56b0d
Inspection Facts
- Inspection number
- 1015650
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Angiplast Private Limited
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2020 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 13, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Angiplast Private Limited
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.