# Lead-Lok Inc – FDA Inspection, Mar 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/lead-lok-inc/b481ff65-f3c3-476e-93da-ce7ef9560249
Source feed: FDA_Inspections

> FDA inspection 1014493 of Lead-Lok Inc, March 28, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014493
- Company Name: Lead-Lok Inc
- Inspection Date: 2017-03-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 871961 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/lead-lok-inc/b8a5067a-081c-4076-b5ec-304034a3db24)
- [FDA Inspection 735990 - 2011-07-11](https://www.keypedia.com/records/fda_inspections/lead-lok-inc/d29484c7-5ad7-479d-aee0-005d559838cf)

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/lead-lok-inc/00b03996-7684-4a34-b906-8d7e98e4845d

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