FDA Intel

Cyalume Technologies, Inc

FDA inspection history in W Springfield, Massachusetts, 2018 to 2022

2
Form 483s

Every document, by year

  • Form 483

2018: one Form 483; 2022: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2018One Form 483, at W Springfield, Massachusetts.
  2. 2022One Form 483, at W Springfield, Massachusetts.
  3. 2022The longest 483 on file: 2 observations over 4 pages at W Springfield, Massachusetts.

Cited most

Across all Cyalume Technologies observations on file

  • 21 CFR 820.30(d)
    Design controls
    2
  • 21 CFR 803.17
    What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
    1

The complete Cyalume Technologies file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2022-10-19483 Form 483$99
2018-08-24483 Form 483$99

Investigators on these documents

Jeffrey J. Thibodeau (2)

FEI number 1000137551 · most recent document Oct 19, 2022

About Cyalume Technologies, Inc

How many FDA Form 483s has Cyalume Technologies, Inc received?

FDA Intel has 2 Form 483s on file for Cyalume Technologies, Inc; the most recent is dated Oct 19, 2022.

When was Cyalume Technologies, Inc last inspected by FDA?

The most recent FDA inspection document on file for Cyalume Technologies, Inc is a Form 483 dated Oct 19, 2022, for the site in W Springfield, Massachusetts.

What did FDA cite at Cyalume Technologies, Inc?

The regulations cited most in the observations on file for Cyalume Technologies, Inc are 21 CFR 820.30(d) (Design controls), 2 times; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time.