# Endotec, Inc. – FDA Inspection, Dec 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/endotec-inc/5429f8e3-54b2-4f9f-9087-08448aba21ad
Source feed: FDA_Inspections

> FDA inspection 1036515 of Endotec, Inc., December 19, 2017. Classification: Official Action Indicated (OAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036515
- Company Name: Endotec, Inc.
- Inspection Date: 2017-12-19
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 991826 - 2016-10-14](https://www.keypedia.com/records/fda_inspections/endotec-inc/54db0071-85db-4bf7-a3e6-3ce002d87dfb)
- [FDA Inspection 743659 - 2011-09-07](https://www.keypedia.com/records/fda_inspections/endotec-inc/f63f2b2b-944d-446c-aa6c-03acb229f732)
- [FDA Inspection 706996 - 2011-01-19](https://www.keypedia.com/records/fda_inspections/endotec-inc/ff176dd4-2fc6-441a-93b0-09bcd887d88c)
- [FDA Inspection 585102 - 2009-05-29](https://www.keypedia.com/records/fda_inspections/endotec-inc/3d416002-c78e-4ed0-bddf-ef54905dc529)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

Company: https://www.keypedia.com/companies/endotec-inc/db3ee6a3-e86b-4cb9-ab17-eeff33ebcfe5

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
