Sciarra Laboratories, Inc
FDA inspection history in Hicksville, New York, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Hicksville, New York.
Cited most
Across all Sciarra Laboratories observations on file
- 21 CFR 211.160(a)General requirements2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Sciarra Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Hicksville, New York
One Form 483 · 2023 · 6 observations
Latest: Form 483, Aug 7, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-08-07 | 483 Form 483 | Hicksville, New York | 6 | $99 |
Investigators on these documents
FEI number 1000306996 · most recent document Aug 7, 2023
About Sciarra Laboratories, Inc
How many FDA Form 483s has Sciarra Laboratories, Inc received?
FDA Intel has 1 Form 483 on file for Sciarra Laboratories, Inc; the most recent is dated Aug 7, 2023.
When was Sciarra Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Sciarra Laboratories, Inc is a Form 483 dated Aug 7, 2023, for the site in Hicksville, New York.
What did FDA cite at Sciarra Laboratories, Inc?
The regulations cited most in the observations on file for Sciarra Laboratories, Inc are 21 CFR 211.160(a) (General requirements), 2 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.