FDA Investigator Gilbert Valdez, RS

Gilbert Valdez, RS has conducted inspections on 21 sites in 1 countries as of 01 May 2023. See below for a list of the FDA enforcement documents resulting from those inspections.

Gilbert Valdez, RS's Documents

Publish Date Document Type Title
January, 2021 FDA 483 Strauman Manufacturing Inc. - Form 483, 2021-01-14
February, 2023 FDA 483 Surgisil, LLP - Form 483, 2023-02-08
April, 2023 FDA 483 DPT Laboratories, Ltd. - Form 483, 2023-04-06
June, 2017 EIR Blickman Inc. - EIR, 2017-06-23
January, 2023 FDA 483 ASPENSTATE, INC - Form 483, 2023-01-26
May, 2023 FDA 483 Slow Wave, Inc. - Form 483, 2023-05-03
September, 2021 FDA 483 CTL Medical Corporation - Form 483, 2021-09-03
December, 2022 FDA 483 Kensington Medical Holdings LLC - Form 483, 2022-12-07
August, 2019 FDA 483 EVOLUTION SPINE, LLC - Form 483, 2019-08-01
December, 2021 FDA 483 Quality Aspirators, Inc - Form 483, 2021-12-02
February, 2023 FDA 483 RSI Technology Group, LLC - Form 483, 2023-02-22
March, 2023 FDA 483 Turnco Tool & Instrument, Inc. - Form 483, 2023-03-16
July, 2018 FDA 483 Alliance Tech Medical, Inc - Form 483, 2018-07-18
November, 2022 FDA 483 Custom Interventional Pain Management, LLC - Form 483, 2022-11-16
February, 2022 FDA 483 Continuity Health Solutions, LLC - Form 483, 2022-02-02
September, 2019 FDA 483 Metric Medical Devices Inc - Form 483, 2019-09-19
July, 2014 EIR Ricca Chemical Company LLC - EIR, 2014-07-23
February, 2019 FDA 483 RadiaDyne LLC - Form 483, 2019-02-27
August, 2021 FDA 483 MJM International Corporation - Form 483, 2021-08-12
February, 2021 FDA 483 MEDHAB - Form 483, 2021-02-11
March, 2022 FDA 483 EINSTEIN WORKS, LLC - Form 483, 2022-03-23
May, 2021 FDA 483 Thompson Ocular Prosthetics, Inc - Form 483, 2021-05-12
December, 2020 FDA 483 Dentlight Inc - Form 483, 2020-12-16

Experience Redica Systems’ NEW investigator profiles and dashboards

Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:

  • Total inspections conducted
  • 483 rate
  • OAI rate
  • Warning Letter rate
  • Inspections by Industry, Scope, and Inspection Reason
  • And much more

Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.

FDA Investigator Profile Icon

Talk to sales to access our investigator profiles

Loading...

Investigator Profiles Are Just the Tip of the Iceberg

Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:

Inspection Intelligence

  • Pre-Approval Inspection (PAI) trends
  • The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
  • Latest 483s: see what the trends are across all FDA Investigators
  • CFR Heatmap: Citations aggregated by Subpart by Year

Vendor Intelligence

  • Full inspection histories for your vendors down to the specific site level
  • All of the functionality mentioned above but isolated to just your vendors

Regulatory Intelligence

  • Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
  • All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more