# HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV, Bangalore, India – FDA Inspections

Source: https://www.keypedia.com/companies/healthium-medtech-private-limited-formerly-sutures-india-pv/e4d651db-4ead-4b6c-b1a1-16e260b305ad

> Inspection records and compliance data for HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV in Bangalore. 3 FDA inspections on record (1 OAI), last inspected April 29, 2016.

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## Details

- Name: HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV
- FEI Number: 3004944585
- Address Line 1: 472 D 13th Cross, 4TH PHASE, PEENYA INDUSTRIAL AREA
- City: Bangalore
- Country Name: India
- Address: 472 D 13th Cross, 4TH PHASE, PEENYA INDUSTRIAL AREA, Bangalore, India
- Country: India

## Related Documents

- [FDA Inspection 986076 - HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV - 2016-04-29](https://www.keypedia.com/records/fda_inspections/healthium-medtech-private-limited-formerly-sutures-india-pv/3b3f1491-920a-41b8-a3eb-87b717fb4c3f) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- FDA Inspection 986076 - HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV - 2016-04-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2016
- [FDA Inspection 811979 - HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV - 2012-12-20](https://www.keypedia.com/records/fda_inspections/healthium-medtech-private-limited-formerly-sutures-india-pv/11e4bd4c-c851-45d6-a802-cfe7cf2267b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2012
- FDA Inspection 662414 - HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV - 2010-04-23 — classification: Official Action Indicated (OAI), source: FDA, date: April 23, 2010
- [FDA Inspection 662414 - HEALTHIUM MEDTECH PRIVATE LIMITED (FORMERLY SUTURES INDIA PV - 2010-04-23](https://www.keypedia.com/records/fda_inspections/healthium-medtech-private-limited-formerly-sutures-india-pv/d2adde70-361e-4dbf-8a89-675304d6e401) — classification: Official Action Indicated (OAI), source: FDA, date: April 23, 2010

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